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FDA-Approved Peanut Immunotherapy Protocol Comes With a Cost – Medscape

Peanut allergy immunotherapy now comes with approval from the US Food and Drug Administration (FDA), but it also comes with protocols, standards, and paperwork. Whether it will be widely adopted has yet to be determined.

A few dozen allergists around the world have been offering food allergy immunotherapy for many years, having developed their own measuring techniques using store-bought food.

But the vast majority of allergists are not interested in developing home-grown treatments, not only because it involves research and development, but also because it comes with legal risks.

"Finally we have another treatment option," said Edwin Kim, MD, from the UNC Allergy and Immunology Clinic in Chapel Hill, North Carolina. "This is what we were waiting for. It's not cowboy stuff; this works."

In January, the FDA approved peanut allergen powder (Palforzia) for patients 4 to 17 years of age, as reported by Medscape Medical News.

The pill contains measured doses of peanut flour and comes with a protocol that will allow allergists to bring patients to a peanut tolerance of 300mg (about onepeanut) and a black-box warning about anaphylaxis risk.

And before allergists can prescribe it, they must take a Risk Evaluation and Mitigation Strategy course to learn about dosing and the allergic reaction protocol.

"That may scare some away," said Kim, who discussed the FDA-approved option during his presentation at the American College of Allergy, Asthma& Immunology 2020 Annual Scientific Meeting.

Allergic reaction, including the potential for anaphylaxis, has always been an issue with immunotherapy.

"People make the argument that there is a difference" between an expected allergic reaction such as one that occurs after the administration of immunotherapy and an unexpected reaction, he said. Because an expected reaction can be treated quickly, "some feel these expected reactions don't matter so much."

"Others say a reaction is a reaction," and argue that if a treatment causes reaction, then it doesn't make sense, he explained.

It comes down to patients they must be willing to take a risk to develop tolerance and improve their quality of life and the allergists willing to treat them.

The peanut powder involves paperwork, preauthorization forms, denials of care, a higher price tag, regimented procedures, and a prerequisite number of visits with patients. "Not everyone will want to do this," said Kim.

This product offers some reassurance, and that matters.

The regimen involves three phases. During initial dose escalation, five doses are administered in the office on day1. Then, over the next 6 months, updoses are administered during 11 in-office sessions and a 300mg tolerance is achieved. Finally, to maintain tolerance to one peanut, daily doses are administered at home.

The drug cost alone is about $4200 a year, according to Institute for Clinical and Economic Review. Peanut flour from the grocery store is cheaper, but comes with the risk of bacteria or other contamination.

"This product offers some reassurance, and that matters," Kim said.

It's good to have more options for food allergy treatment. "We need a more proactive way to treat food allergy; avoidance is not good enough," he explained. "And presumably, at some point, the patient will be able to eat a grocery-store peanut instead of buying the pills."

But not all allergists will be able to make the protocol work. And it's not clear whether there is room to alter treatment and offer patients with a higher tolerance a higher starting dose. What we do know, though, is that "the product leaves little room for 'the art of medicine'," Kim said.

That art is practiced by Arnon Elizur, MD, from the Shamir Medical Center in Tzrifin, Israel, but it's backed by a rigid home-grown protocol.

Since 2010, he has treated 1800 patients for peanut allergy, updosing slowly to a tolerance of 3000mg of peanut, the equivalent of 10 peanuts. He keeps the maintenance dose at four peanuts (1200mg). His center takes a personalized approach, starting patients on the highest dose they can tolerate and working up, with daily patient check-ins from home and a staff available around the clock to answer questions and deal with reactions.

"We aim for full sensitization," Elizur told Medscape Medical News.

The peanut pill is "a big step forward" for immunotherapy, he said. It is "a standardized product, checked for bacteria and allergen content, which is available to a wide community of physicians."

But, he pointed out, "it's expensive." And it's only for peanut. "There are millions of food-allergic patients around the world dying from adverse reactions to many different kinds of food. We don't want to wait for years for a product for all of them. We can use the actual food."

He questions the lifelong maintenance protocol with a daily 300mg pill. "If you can't eat a peanut, why would you buy a drug that's a peanut?" he asked.

He also said he's disappointed that the product is not indicated for adults.

At the Shamir clinic, reactions are closely monitored. "Some are mild, others we treat with autoinjectors, epinephrine," he reported. "Those are the most undesirable."

Data from his center show that reactions occur in about 15% of patients. But his treatment success rates are good. In an average of 8 months, he is able to get 80% of his adult patients to full sensitization.

But it's not for all patients or for all clinics, he acknowledged. "We continue to look at this balance in quality of life throughout the process. Our goal is to improve the quality-of-life threshold."

Treatment that involves "native food" is "a lot of work" and requires "a lot of investment," Elizur said. His center uses a web reporting system to maintain a 24/7 dialog with patients, "and we look at the reports every day." They also have a physician on call at all times. "Not everyone can commit to providing care throughout the day and night."

His center charges the equivalent of $US3000 per food allergy treated. "That's whether it takes 6 months or 2 years," he said.

There are more than 1000 people on his 3-year waiting list.

Immunotherapy is not easy to do, whether it's FDA-approved or not.

"This is the first year that the American College of Allergy, Asthma, and Immunology is not hosting a procon debate on oral immunotherapy," Kim pointed out. "We have a therapy now."

However, the pandemic has slowed treatment uptake. "Immunotherapy is not easy to do, whether it's FDA-approved or not," he explained. With at least 11 doctor visits in the first 6 months each visit is between 30 minutes and 2 to 3 hours it hasn't been possible to set up this year. "It's not ideal."

It will be interesting to see "how this will roll out and how it will be adopted," Kim said. "From a food allergy point of view, the next 12 months are going to be very interesting."

Kim reports receiving consulting honorarium from Aimmune, the maker of Palforzia; being on the clinical medical advisory board for DBV Technologies; and consulting for DBV, Aimmune, Allakos, Allergenis, Ukko Incorporated, Vibrant America, Duke Clinical Research Institute, and Kenota Health. Elizur has The disclosed no relevant financial relationships.

American College of Allergy, Asthma & Immunology (ACAAI) 2020 Annual Scientific Meeting.

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FDA-Approved Peanut Immunotherapy Protocol Comes With a Cost - Medscape

RAPT Therapeutics Reports Positive Initial Data from Ongoing Phase 1/2 Clinical Trial of FLX475 in Multiple Cancer Indications – BioSpace

-Evidence of Monotherapy and Combination Activity in Charged Tumor Types--Company Advances Several Cohorts into Phase 2 Expansions--Conference Call and Webcast to be Held at 8:30 a.m. ET Today-

SOUTH SAN FRANCISCO, Calif., Nov. 16, 2020 (GLOBE NEWSWIRE) -- RAPT Therapeutics, Inc.. (Nasdaq: RAPT), a clinical-stage, immunology-based biopharmaceutical companyfocused on discovering, developing and commercializing oral small molecule therapies for patients with significant unmet needs in oncology and inflammatory diseases, today announced positive initial clinical data from its ongoing Phase 1/2 trial for FLX475 in multiple cancer indications.

Initial observations as of November 10, 2020 from the ongoing trial for FLX475 include preliminary:

In addition, FLX475 demonstrated a favorable safety profile, both as monotherapy and in combination with pembrolizumab.

We are pleased with the early evidence of clinical activity of FLX475, both as monotherapy and in combination with pembrolizumab in multiple charged tumor types, said Brian Wong, M.D., Ph.D., President and CEO of RAPT. Based on these encouraging data, we have determined that three cancer indications, EBV+ lymphoma, nasopharyngeal cancer and head and neck cancer, have generated sufficient early evidence of efficacy to advance into expanded Phase 2 evaluation. We continue to enroll patients and generate data in this multi-cohort, multi-indication trial and look forward to providing updates on all remaining cohorts and additional go-forward decisions next year.

Scott Antonia, M.D., PhD., Professor of Medicine and Director of the Duke Cancer Institute Center for Cancer Immunotherapy and a member of RAPTs Scientific Advisory Board, added, FLX475 is a potent non-depleting CCR4 antagonist that is designed to block regulatory T cells that interfere with an effective anti-tumor immune response. These data are particularly impressive as the immunotherapy field has long recognized Treg as important targets in oncology, but until FLX475, others have not been able to selectively target these cells in the tumor microenvironment without affecting beneficial cells. These data demonstrate that RAPTs oral small molecule approach with FLX475 holds promise in treating a variety of charged cancers.

Charged cancers are tumors that contain high levels of both regulatory T cells (Treg) and CD8 T cells and express high levels of the ligands for CCR4.

Phase 1/2 Clinical Trial DesignThe ongoing open-label Phase 1/2 study is enrolling patients with multiple types of cancer at leading cancer centers across the United States, Australia and Asia. The Phase 1 portion of the trial is focused on evaluating the safety, pharmacokinetics and pharmacodynamics of FLX475 as a monotherapy and in combination with pembrolizumab. The Phase 2 portion is designed to evaluate the degree of antitumor activity of FLX475 as a monotherapy and in combination with pembrolizumab specifically in patients with several types of charged tumors. Changes in the tumor microenvironment and other biomarkers are being evaluated in both phases of the study. For more information please visit clinicaltrials.gov identifierNCT03674567.

Phase 1 Dose Escalation DataThe dose escalation Phase 1 portion of the trial enrolled a total of 37 patients with cancers of different types. Nineteen patients were treated with one of four doses (25 mg, 50 mg, 75 mg or 100 mg once daily) of FLX475 monotherapy and 18 were treated with one of three doses (50 mg, 75 mg or 100 mg once daily) of FLX475 in combination with the standard dose of pembrolizumab. Disease control, defined as a best response of stable disease (SD), an unconfirmed or confirmed partial response (PR) or complete response (CR), was observed in 14 of the 17 evaluable monotherapy patients, including an unconfirmed partial response in a patient with relapsed metastatic cervical cancer. In the combination cohorts, disease control was observed in 13 of the 14 evaluable patients. This includes two confirmed partial responses: a patient with NSCLC who had progressed on prior checkpoint treatment (atezolizumab) and who remains on study after 18 months of treatment, and a patient with checkpoint inhibitor-nave urothelial cancer who was on study for over nine months of treatment. In addition, preliminary data show an increase in the CD8 to Treg ratio after treatment, which is consistent with the hypothesis that a CCR4 antagonist can block the recruitment of tumor Treg, increase the CD8 to Treg ratio and potentially enhance antitumor immunity.

The Phase 1 results also show FLX475 had a favorable safety profile, with no maximum tolerated dose reached. Two dose-limiting toxicities (DLTs) of asymptomatic QTc prolongation were observed in the monotherapy cohorts, one in the 75 mg cohort and one in the 100 mg cohort. No DLTs were observed in the Phase 1 combination cohorts. Based on the Phase 1 data, 100 mg was selected as the recommended Phase 2 dose for both the monotherapy and combination therapy cohorts.

Phase 2 DataThe ongoing Phase2 portion of the trial is enrolling a minimum of 80 patients with several types of charged tumors, 10 in each of eight cohorts, with four cohorts evaluating FLX475 as a monotherapy and four cohorts evaluating FLX475 in combination with pembrolizumab. The charged cancers include Epstein-Barr Virus (EBV)- or Human Papillomavirus (HPV)-associated cancers such as nasopharyngeal cancer, cervical cancer, and subsets of Hodgkin and non-Hodgkin lymphomas as well as head and neck cancer. Other charged tumor types include non-small cell lung cancer and triple-negative breast cancer. The protocol calls for expansion of cohorts to generate additional data based on promising clinical activity.

Based on the promising early results from the Phase 1/2 trial with FLX475 observed to date, RAPT has selected three cancer indications for expansion:

In these Phase 2 cohorts, FLX475 demonstrated a favorable safety profile with once-daily oral dosing both as monotherapy and in combination with pembrolizumab.

a Interim data as of November 10, 2020 from the ongoing FLX475-02 Phase 1/2 study; data subject to change.bORR = objective response rate defined as unconfirmed and confirmed PR or CRcDCR = disease control rate defined as unconfirmed and confirmed PR or CR and SD as best response

Conference Call InformationThe Company will host a webcast conference call accompanied by a slide presentation to discuss initial data from the Phase 1/2 study of FLX475 today at 8:30 a.m. Eastern Time. The call can be accessed by dialing (833) 672-0665 (domestic) or (929) 517-0344 (international) and refer to conference ID 6772479. The webcast will be available for replay for two weeks.

About FLX475FLX475 is a small molecule CCR4 antagonist designed to block the migration of regulatory T cells (Treg) specifically into tumors, but not healthy tissues. Tregrepresent a dominant pathway for downregulating the immune response, generally correlate with poor clinical outcomes and may limit the effectiveness of currently available therapies such as checkpoint inhibitors. RAPT is developing FLX475 for the treatment of a broad range of charged tumors, which represent cancer types the Company believes are most likely to respond to FLX475, where a large quantity of Tregcells are likely to be the cause of immune suppression within the tumor. FLX475 may restore naturally occurring antitumor immunity alone and may synergize with a variety of both conventional and immune-based therapies, such as radiation, chemotherapy, checkpoint inhibitors, immune stimulators, cancer vaccines and adoptive T cell therapy.

AboutRAPT Therapeutics, Inc.RAPT Therapeutics is a clinical stage immunology-based biopharmaceutical company focused on discovering, developing and commercializing oral small molecule therapies for patients with significant unmet needs in oncology and inflammatory diseases. Utilizing its proprietary discovery and development engine, the Company is developing highly selective small molecules designed to modulate the critical immune drivers underlying these diseases. RAPT has discovered and advanced two unique drug candidates, FLX475 and RPT193, each targeting C-C motif chemokine receptor 4 (CCR4), for the treatment of cancer and inflammation, respectively. The Company is also pursuing a range of targets, including hematopoietic progenitor kinase 1 (HPK1) and general control nonderepressible 2 (GCN2), that are in the discovery stage of development.

Forward-Looking StatementsThis press release contains forward-looking statements. These statements relate to future events and involve known and unknown risks, uncertainties and other factors that may cause our actual results, performance or achievements to be materially different from any future performances or achievements expressed or implied by the forward-looking statements. Each of these statements is based only on current information, assumptions and expectations that are inherently subject to change and involve a number of risks and uncertainties. Forward-looking statements include, but are not limited to, statements about clinical development progress, the significance of early results from Phase 1/2 clinical trials of FLX475 and plans with respect to Phase 2 expansions. Detailed information regarding risk factors that may cause actual results to differ materially from the results expressed or implied by statements in this press release may be found in RAPTs most recent Form 10-Q filed with the Securities and Exchange Commission and subsequent filings made by RAPT with the Securities and Exchange Commission. These forward-looking statements speak only as of the date hereof. RAPT disclaims any obligation to update these forward-looking statements.

RAPT Media Contact:Angela Bittingmedia@rapt.com(925) 202-6211

RAPT Investor Contact:Sylvia Wheelerswheeler@wheelhouselsa.com

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RAPT Therapeutics Reports Positive Initial Data from Ongoing Phase 1/2 Clinical Trial of FLX475 in Multiple Cancer Indications - BioSpace

RAPT Therapeutics Reports Third Quarter 2020 Financial Results – BioSpace

SOUTH SAN FRANCISCO, Calif., Nov. 16, 2020 (GLOBE NEWSWIRE) -- RAPT Therapeutics, Inc.. (Nasdaq: RAPT), a clinical-stage, immunology-based biopharmaceutical companyfocused on discovering, developing and commercializing oral small molecule therapies for patients with significant unmet needs in oncology and inflammatory diseases, today reported financial results for the third quarter ended September 30, 2020 and provided an update on recent operational and business progress.

Earlier today, we reported positive initial data from our ongoing Phase 1/2 clinical trial evaluating FLX475 in multiple cancer indications, said Brian Wong, M.D., Ph.D., President and CEO of RAPT Therapeutics. With the advancement of this program and continued enrollment for our ongoing Phase 1b study of RPT193 in atopic dermatitis, which we now expect to read out in the first half of 2021, we are well positioned for multiple catalysts in 2021.

Financial Results for the Third Quarter and Nine Months Ended September 30, 2020

Third Quarter Ended September 30, 2020Net loss for the third quarter of 2020 was $14.6 million, compared to $10.0 million for the third quarter of 2019.

Research and development expenses for the third quarter of 2020 were $12.9 million, compared to $8.6 million for the same period in 2019 due to increased clinical costs for FLX475 and RPT193, increased personnel costs and stock-based compensation expense, an increase in preclinical program costs and laboratory supplies.

General and administrative expenses for the third quarter of 2020 were $3.2million, compared to $1.7million for the same period of 2019. The increase was primarily due to an increase in stock-based compensation expense, personnel costs, legal and accounting fees and insurance expense offset by a decrease in consulting costs.

Nine Months Ended September 30, 2020Net loss for the nine months ended September 30, 2020 was $40.2 million, compared to $29.8 million for the same period in 2019.

Research and development expenses for the nine months ended September 30, 2020 were $34.6 million, compared to $24.7 million for the same period in 2019. The increase was primarily due to an increase in clinical costs relating to FLX475 and RPT193, increased preclinical program costs as well as increased stock-based compensation and personnel expenses, offset by decreases in lab supplies and travel costs.

General and administrative expenses for the nine months ended September 30, 2020 were $9.3million, compared to $6.1million for the same period of 2019. The increase in general and administrative expenses was primarily due to increased stock-based compensation expense, increased personnel costs, an increase in legal and accounting fees as well as insurance expense offset by a decrease in travel and consulting costs.

As of September 30, 2020, we had cash and cash equivalents and marketable securities of $122.8 million.

AboutRAPT Therapeutics, Inc.RAPT Therapeutics is a clinical stage immunology-based biopharmaceutical company focused on discovering, developing and commercializing oral small molecule therapies for patients with significant unmet needs in oncology and inflammatory diseases. Utilizing its proprietary discovery and development engine, the Company is developing highly selective small molecules designed to modulate the critical immune drivers underlying these diseases. RAPT has discovered and advanced two unique drug candidates, FLX475 and RPT193, each targeting C-C motif chemokine receptor 4 (CCR4), for the treatment of cancer and inflammation, respectively. The Company is also pursuing a range of targets, including hematopoietic progenitor kinase 1 (HPK1) and general control nonderepressible 2 (GCN2), that are in the discovery stage of development.

Forward-Looking StatementsThis press release contains forward-looking statements. These statements relate to future events and involve known and unknown risks, uncertainties and other factors that may cause our actual results, performance or achievements to be materially different from any future performances or achievements expressed or implied by the forward-looking statements. Each of these statements is based only on current information, assumptions and expectations that are inherently subject to change and involve a number of risks and uncertainties. Forward-looking statements include, but are not limited to, statements about clinical development progress and the timing of results from clinical trials of FLX475 and RPT193. Detailed information regarding risk factors that may cause actual results to differ materially from the results expressed or implied by statements in this press release may be found in RAPTs most recent Form 10-Q filed with the Securities and Exchange Commission and subsequent filings made by RAPT with the Securities and Exchange Commission. These forward-looking statements speak only as of the date hereof. RAPT disclaims any obligation to update these forward-looking statements.

RAPT Media Contact:Angela Bittingmedia@rapt.com(925) 202-6211

RAPT Investor Contact:Sylvia Wheelerswheeler@wheelhouselsa.com

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RAPT Therapeutics Reports Third Quarter 2020 Financial Results - BioSpace

Study reveals key role of IL-33 signaling molecule in parasite infections, other health conditions – News-Medical.Net

Reviewed by Emily Henderson, B.Sc.Nov 15 2020

De'Broski Herbert has a philosophy that's guided his career researching helminths, or parasitic worms, and their interaction with their hosts' immune systems: "Follow the worm."

The mantra of my lab since its inception has been that parasitic worms manipulate their hosts in very interesting ways to maintain their survival. SARS-CoV-2 doesn't care about staying in your body very long because it is transmitted so easily. Worms aren't spread so easily, so they have to figure out how to persist."

De'Broski Herbert, Asociate Professor of Pathobiology, School of Veterinary Medicine, University of Pennsylvania

That focus has revealed a key insight about an immune signaling molecule, the cytokine IL-33, that is important not only in parasite infections, but in a range of other health conditions, such as asthma, obesity, and eczema.

In a new study published in Science Immunology, Herbert and colleagues made insights that explain how IL-33 can both help defend the body against parasite infection, but also suppress chronic inflammation in diseases where the immune system is activated inappropriately and causes harmful pathology. A key discovery was that the activity of IL-33 depends upon which cell type is releasing it.

"Lots of people have been interested in IL-33 ever since two big genomic association studies implicated it and its receptor in the pathogenesis of asthma," Herbert says. "Other researchers have looked at it in the context of infections and others in the context of the brain and development. And everyone knew this protein was in the nucleus, but no one understood how it got out of the cell to accomplish all of these things.

"I'm excited for this work because not only do we find this cytokine in a cell type that nobody was expecting, but we also present a mechanism that no one was expecting for how it could come out."

IL-33 has been of major interest to immunologists focused on what are known as type 2 immune responses, typically associated with parasite infections or asthma and allergies.

On the parasite front, researchers knew that IL-33 acted in part to "wake up" the immune system to the presence of a worm infection. In a mouse model, animals lacking IL-33 sustain worm infections much longer than those with IL-33 intact.

To find out whether it mattered which cell type was releasing the IL-33 signaling molecule, Herbert and colleagues used special mouse model in which only myeloid antigen-presenting cells (immune cells), or epithelial cells (those that line mucosal surfaces), failed to release IL-33.

"Sure enough, we found that when animals lacking the myeloid-derived IL-33 experienced a hookworm infection, they eliminated those hookworms quite fast," Herbert says.

Mice lacking IL-33 in the epithelial cells, however, were not able to readily clear the infection. The same results held up in another rodent model, this one of roundworm infection.

Dendritic cells, a type of myeloid antigen-presenting cell, produce IL-33, and further experiments showed that the cytokine produced by these cells supported a specific population of regulatory T cells (Tregs), which are cells "whose whole purpose is to suppress the immune response," Herbert says.

Now understanding that dendritic cells were key to supporting Tregs, the researchers wanted to understand how the dendritic cells were delivering the IL-33. The team screened dendritic cells from mice with and without IL-33, identifying a protein called perforin-2 to be suppressed in expression from myeloid cells lacking IL-33.

Perforin-2, as its name suggests, forms a pore that spans the cell membrane, like a tunnel in a hillside, allowing the transport of proteins in and out.

The find made complete sense to the researchers, providing an explanation for how dendritic cells could promote the release of IL-33 into the tissues to interact with Tregs. And when Herbert and colleagues experimentally eliminated perforin-2 from dendritic cells, they saw a subsequent lack of Treg growth.

To connect the findings in their animal model and lab dishes to humans, the team utilized patient samples from Penn otolaryngologist Noam Cohen.

They found perforin-2 at the plasma membrane of cells from polyps removed from patients with chronic rhinosinusitis, suggesting that the significance of the findings extends to human health.

The study paves the way for even more translational work in immunology--and worms are to thank. "It's kind of the missing link," Herbert says. "It opens up a whole new direction for understanding how this cytokine could be involved in obesty, inflammatory bowel disease, Crohn's, asthma, and development."

Source:

Journal reference:

Hung, L-Y., et al. (2020) Cellular context of IL-33 expression dictates impact on anti-helminth immunity. Science Immunology. doi.org/10.1126/sciimmunol.abc6259.

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Study reveals key role of IL-33 signaling molecule in parasite infections, other health conditions - News-Medical.Net

RAPT Therapeutics to Announce Initial Data from Phase 1/2 Clinical Trial of FLX475 in Multiple Cancer Indications – BioSpace

SOUTH SAN FRANCISCO, Calif., Nov. 15, 2020 (GLOBE NEWSWIRE) -- RAPT Therapeutics, Inc. (Nasdaq: RAPT), a clinical-stage, immunology-based biopharmaceutical company focused on discovering, developing and commercializing oral small molecule therapies for patients with significant unmet needs in oncology and inflammatory diseases, today announced that the Company plans to present initial data from its Phase 1/2 clinical trial of FLX475 in patients with multiple cancer indications in a premarket press release and webcast on Monday, November 16, 2020.

RAPT will host a conference call accompanied by a slide presentation at 8:30 a.m. ET on Monday, November 16th. The live webcast and audio archive of the presentation may be accessed on the RAPT Therapeutics website at https://investors.rapt.com/events-and-presentations. The call can be accessed by dialing (833) 672-0665 (domestic) or (929) 517-0344 (international) and refer to conference ID 6772479. The webcast will be available for replay for two weeks. Please connect to the website 10 minutes prior to the presentation to ensure adequate time for any software downloads that may be necessary to listen to the webcast.

About RAPT Therapeutics, Inc.RAPT Therapeutics is a clinical stage immunology-based biopharmaceutical company focused on discovering, developing and commercializing oral small molecule therapies for patients with significant unmet needs in oncology and inflammatory diseases. Utilizing its proprietary discovery and development engine, the Company is developing highly selective small molecules designed to modulate the critical immune drivers underlying these diseases. RAPT has discovered and advanced two unique drug candidates, FLX475 and RPT193, each targeting C-C motif chemokine receptor 4 (CCR4), for the treatment of cancer and inflammation, respectively. The Company is also pursuing a range of targets, including hematopoietic progenitor kinase 1 (HPK1) and general control nonderepressible 2 (GCN2), that are in the discovery stage of development.

RAPT Media Contact:Angela Bittingmedia@rapt.com(925) 202-6211

RAPT Investor Contact:Sylvia Wheelerswheeler@wheelhouselsa.com

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RAPT Therapeutics to Announce Initial Data from Phase 1/2 Clinical Trial of FLX475 in Multiple Cancer Indications - BioSpace

Anatomy of a Play: The hidden design behind the Cardinals’ ‘Hail Murray’ miracle – Touchdown Wire

The term Hail Mary in a football sense was probably invented by Elmer Layden and Jim Crowley, two members of Notre Dames Four Horsemen backfield, in the 1930s. The more common origination of the desperation pass came in a divisional playoff game between the Cowboys and Vikings in 1975, when Roger Staubach heaved up a pass to receiver Drew Pearson with little time left, and Pearson caught it for the winning score.

(Never mind what looked to be uncalled offensive pass interference on the play; were talking about NFL history here).

I closed my eyes and said a Hail Mary. Staubach said years later.

Fast forward to the Cardinals 32-30 win over the Bills on Sunday, when the name changed to Hail Murray after Arizona quarterback Kyler Murray broke the pocket, moved to his left, and made an incredible throw falling away from the target. The play started with 11 seconds left on the clock and Buffalo up, 30-26.

Here, as you all know by now, is how it ended.

Receiver DeAndre Hopkins out-leaped three Bills defenders, including TreDavious White, the teams best cornerback, and Micah Hyde and Jordan Poyer, the teams two best safeties. He came down with one of the great successful desperation catches of all time, and that was that for the Bills. The Cardinals, for their reward, now own first place in the NFC West at 6-3.

On the game-winning drive, Murray completed all four of his passes to three different receivers (Hopkins, Larry Fitzgerald, and Andy Isabella) for 75 yards. The Cardinals were in 10 personnel for all four plays four receivers, no tight ends, and running back Chase Edmonds in this case. This should have come as no surprise. Per Sharp Football Stats, Arizona came into this game with the NFLs highest percentage of 10 personnel on 21% of their offensive plays. Murray had completed 50 of 79 passes for five touchdowns, two interceptions, and a passer rating of 90.2 out of 10 personnel numbers that were about to get a lot better.

The Cardinals wanted to move quickly, so they ran two concepts out of 10 empty backfields on the first two plays, and three-by-one sets on the last two. The three-by-one set forced the Bills to slant their coverage to the three-receiver side, with Hopkins as the iso receiver to the field.

On the most consequential play, the Bills are playing a nickel defense (five defensive backs and linebacker Tremaine Edmonds), giving them the best possible matchup for whatever manner of magic Murray is about to try and create. White has Hopkins all the way down the field, Hyde drifts over to help after scanning the middle of the field, and Poyer jumps in late to try and add a body.

Not that any of that mattered.

When I got ready to take the snap, Im trying to diagnose the defense, see if theres any holes, Murray told NBC Sports Peter King after the game. Anything easy. I still figured I probably had two plays, two shots at it. The play was designed to roll out left, like I said, and they did a good job of containing,

The rollout left put the onus on Hopkins to get open. The only other throw that would have made sense in this case was the deep over to Fitzgerald from right to left. That probably wouldnt have been a touchdown, and Fitzgerald would have to have gotten out of bounds on a long-developing play, somehow leaving any time on the clock. If that was a planned rollout, head coach and offensive play-designer Kliff Kingsbury was trying to cut the field in half for his quarterback.

I looked downfield, I locked in on Hop. And what was weird was, he was the only player on our team in the end zone, Murray continued. He would obviously have preferred more of his own guys in the end zone to increase the odds of a Cardinals player coming up with the ball.

Hopkins told King that he relied on a martial-arts background of sorts.

My brother and I used to watch a lot of Jet Li movies, so we used to always do quick things like kickboxing or catching things with our hands. One thing I remember we always used to dowe always used to catch flies with our hands. I was the only one that could catch them. I actually studied it, and I grew with it. I was like, How do I catch flies? Flies always fly up. I would always just hit over it. And I thought: If I can catch flies, I know I can catch anything.

As Mr. Miyagi often said.

Murray said that he hadnt thrown many Hail Marys in his life, but hell never forget this.

In high school we had a lot of moments. Never like this one, though. Last-second, I mean, this is the highest level. I really have had a lot of moments in my life but this one, none can compare.

In the moment, you had a coach who knew where his quarterback was most comfortable, a quarterback capable of making the play as few other NFL quarterbacks would have been, and a receiver who was ready to all Jet Li on everyone in a Bills uniform. Thats how the most remarkable play of the 2020 season so far came about.

Luck is the residue of design is a quote attributed to both John Milton and Branch Rickey, but its okay if the Cardinals want to rent it for a while. They certainly earned that right on Sunday.

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Anatomy of a Play: The hidden design behind the Cardinals' 'Hail Murray' miracle - Touchdown Wire

Anatomy Of An Upset: How The Patriots Beat The Ravens – CBS Boston

ByMichael Hurley, CBS Boston

BOSTON (CBS) Figure this one out: A year ago, the Patriots had the best defense in the NFL, yet they got run over by the Baltimore Ravens.

This year, the Patriots entered Sunday night with one of the worst run defenses in the league and a bottom-third overall defense. Yet they somehow put together a tremendous performance in slowing down Lamar Jackson and the leagues No. 1 rushing offense and pulled off the upset victory.

Given the way things were going for the Patriots with a four-game losing streak followed by a nail-biting win against the winless Jets there werent many folks who believedthisupset was possible.

Heres how it happened.

Response

The Patriots fell behind early in the second quarter. They fell behind again just minutes after tying it up. In both instances, they answered with authority.

Following the Ravens endless touchdown drive (13 plays, 94 yards, 8:04), Cam Newton and Co. came right back with a marathon drive of their own. With a 19-yard pass to Jakobi Meyers and a rare 20-yard connection from Newton to Ryan Izzo, the Patriots scored with ease on a first-and-goal play from the 7-yard line. NKeal Harry set a perfect and legal block to spring Rex Burkhead for six.

After a Baltimore field goal, the Patriots once again answered, this time with a 10-play, 75-yard drive to take a lead. Theyd never give it back.

Playing from behind against Baltimore is a recipe for disaster. But those drives coming right after Baltimore scored flipped the script and changed the game.

Red Zone D

That field goal drive by Baltimore wasactuallykind of a loss for the Ravens, as they had driven to the New England 6-yard line. But on third-and-6, the Patriots forced an incompletion, forcing Baltimore to settle for a 24-yard field goal.

The Ravens did reach the end zone on their other two red zone trips, but that stop at that time was critical.

Ball Security

The Ravens certainly had no intention of heading into halftime trailing 13-10. So despite limited time left, they mounted an aggressive drive to try to at least get the tying field goal on the board.

They made it as far as the Patriots 38-yard line before Jackson went for it all, launching a deep bomb up the right sideline to Marquise Brown. Thats when Mr. Interception himself, J.C. Jackson, made sure that Baltimore wouldnotbe adding points before the break.

As that tweet notes, this was the fifth straight game with a pick for Jackson. And it was a big one.

The Patriots also had zero fumbles all night, despite the rainy conditions, and Newton threw no interceptions. The Ravens recovered all three of their fumbles, which all came on bad snaps, but they lost 27 yards in the process. One of those bad snaps came on a fourth down attempt, essentially serving as a turnover.

Damien Harris told reporters after the game that hemighthave played in the rain during his college career once, but it was nothing like the rain that fell on Sunday night. Despite that lack of experience, Harris held on to the ball on all 22 of his carries, rushing for 121 yards as the teams offensive MVP.

We had a couple close calls with trying to gather the snap. Obviously, it was a factor for them, Newton said after the 23-17 win.But having the mentality to stay mentally tough throughout that whole tsunami it felt like, we just wanted to make sure that we do great things while we have the football protecting the football, making great decisions.

Trickery

In a span of about five minutes, the whole world got whacked over the head with the information that Jakobi Meyers used to be a quarterback. But clearly, that wasnt the worlds most well-known tidbit prior to Josh McDaniels and Bill Belichick pulling the trigger on some trickery.

Really, the trick part of Meyers touchdown pass to Rex Burkhead didnt really work, as Patrick Queen was tight in coverage on Burkhead. It was, simply, a tremendous pass and an even better catch.

A trick play or a gadget play or really anything other than a standard football play is always a risky call. If it doesnt work out, all the critics come out with pitchforks and question why the call was made.

But when they work, they create some special moments. Add this one to that list.

Defense

It goes without saying, but you cant beat the Ravens if you cant stop Lamar. Or, more accurately, limit Lamar.

The Patriots did that. He did rush for 55 yards, but he didnt break any runs longer than 11 yards, and he didnt find the end zone. And while his passing numbers were good (24-for-34, 249 yards, 2 TDs, 1 INT), it really wasnt an impactful performance from the reigning MVP.

Bulking up the secondary with Kyle Dugger helped, as the rookie led the team with 12 total tackles (seven solo). John Simon was disruptive in the backfield, recording a sack and batting a pass down. Jason McCourty broke up a pass on a third down, as did his twin brother Devin. Rookie Josh Uche also had a sack the first of his career. Terez Hall was once again actively involved with JaWhaun Bentley out.

It was a team performance, and it ought to be a good day or two in the video room when the defense looks over this film.

Weather

One cant help but think that the Ravens last-gasp drive in the final minute of the fourth quarter might have been different if not for a 10-year storm rolling through Foxboro at that exact moment. While the rain was falling all night, the dial turned to 11 for that final drive somewhat reminiscent of the Patriots loss in Cincinnati during the 2013 season.

The Ravens took over at their own 22-yard line with 1:05 left in the game. They needed a touchdown and a PAT to win the game. They had no timeouts, but a win was still very much in reach. (The Arizona Cardinals provided proof of that earlier in the day.)

Despite that situation, the Ravens really didnt look like they believed they had a chance. A few short completions drained the clock further, before Dugger alertly tackled J.K. Dobbins before the running back could get out of bounds. That brought the clock down to single digits, and on the next snap, Dobbins dropped a pass that hit him directly in the hands. That incompletion resulted in a turnover on downs, ending the game.

Conspiracy theorists will likely suggest that Bill Belichick somehow negotiated the precipitation to increase at that precise moment, but the reality is that the weather is the weather. Sometimes it hurts you, sometimes it gives you a break. For that particular drive, the Ravens got a rough deal.

The weather wasnt on our side, Lamar Jackson said. Every time we was up, it was like the rain just started pouring down even harder. But you know, its part of football. Things happen. The weathers not always going to be perfect, and we still have to find a way to pull out a victory. We just didnt tonight.

You canemail Michael Hurleyor find him on Twitter@michaelFhurley.

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Anatomy Of An Upset: How The Patriots Beat The Ravens - CBS Boston

Dissecting Manipurs anatomy of conflict – The Statesman

The last thing one expects of an Indian conflict zone is an unabashed story from a retired police officer about inter-forces rivalries and human rights controversies. Vale of Tears is one such chilling account by John S Shilshi. It is not only about conflict in the North-eastern states but also the human condition there. The author served in the police force during the height of violent insurgency, ethnic and communal clashes in Manipur. Published by Blue Rose, the book is an anecdotal memoir that offers the reader a peek into the other side of conflict, one that is not found in the public domain.

An Indian Police Service officer of the Manipur cadre, Shilshi served in the ultra-sensitive areas of the state between 1990 and 2000. Trained in counterinsurgency and counterterrorism, he led the elite civil police commando unit during his tenure. The recipient of a gallantry medal for meritorious and distinguished service, he also served in the Intelligence Bureau and the National Security Council Secretariat.

Shilshis upright and unbiased first-hand accounts are like a dissection of the anatomy of Manipurs conflict. There are some rare insights into how the security forces interact with one another in a union of states like India. There are also insights into the friction between the state police and central forces. His investigation of how incidents flare up provides an understanding of the causes, consequences and lessons learnt.

During his tenure, Shilshi witnessed some of the bloodiest incidents of Manipurs violent contemporary history. He stood firm on his principles, often putting his life and job at risk. For instance, when he was posted in Ukhrul a place where many senior members of the National Socialist Council of Nagalim (IsakMuivah) operate from and also the home of its founder-general secretary Th Muivah a notsopleasant encounter took place when a Captain of the Indian Army demanded that he hand over a person picked up by the police. The said person was providing shelter to a NSCN (I-M) man arrested by the Army. This did not go down well with Shilshi. He challenged the Army Captain to knock the doors of the authority, if he dares. The author recalls his conversation with the Captain, Under the law, the police are not duty-bound to hand over any suspect or criminal except in court. Shilshi says, I offered to interrogate the person inside the police station. It was mistaken as favouring the suspect.

Neither did the Captain interrogate the said person nor hand over the arrested NSCN (I-M) man to the police. The Naga Peoples Movement for Human Rights and other rights groups were preparing to file habeas corpus cases before the Imphal bench of Gauhati High Court. Shilshi told the Brigadier that if the court entertained their prayers, his presence would be required and it may not be a pleasant experience. The adamant Brigadier defended himself by saying that the NSCN man was not medically fit to be handed over. Shilshi knew quite well what the repercussion would be if he took the man and he died in his custody. Yet, I went with my gut feeling. Ultimately, the badly bruised NSCN (IM) leader, with several marks and cuts on his body, was received by the officer in charge of Ukhrul Police Station. He was given medical treatment at the 1st Manipur rifle unit hospital, recalls Shilshi.

The 1990s saw the longest and most gruesome ethnic clash between the Nagas and Kukis, where hundreds died on both sides besides several homes and properties being burned or destroyed. As a police officer witnessing some of the incidents, Shilshi observes that even during the peak of the ethnic war, neither a bullet nor an arrow was exchanged, or a spear hurled by common people from both tribes.

According to the author, the attacks were carried out by automatic weapon-wielding men on both sides the Naga Lim Guard and Kuki Defence Force, suspected to be cadres of the NSCN (I-M) and Kuki National Army respectively. Both claimed that the cadres were mobilised to protect and safeguard vulnerable sections of their tribes. Shilshi observes, however, that there were hardly any instances when the armed cadre groups targeted each other directly. Those so-called vanguards of their communitys safety never confronted each other face-to-face. On the contrary, attacks were carried out in farflung areas, butchering helpless and defenceless villagers. Shilshi says, Despite both groups being so well equipped, why were the outfits unable to prevent heinous attacks on their tribesmen/women?

In his account, Shilshi writes that at that point in time the state had nine Manipur Rifles battalions, and two India Reserve Battalions, totalling about 8,800 MR/IRB personnel. Besides them, there were the central forces Army, Assam Rifles and CRPF whose service could have been utilised. Not only were there intelligence inputs, there were open threats and quit notices. But no proactive moves were undertaken to prevent such tragedies, writes Shilshi. The casualties rose from 13 in 1992 to 321 in 1993. It was a loud alarm for the state but unfortunately no action was taken, rues Shilshi.

The authors narration of incidents and his investigative observations bring out some startling revelations. Shilshi found that the late 1990s saw a paradigm shift in the pattern of violence, particularly in urban areas. The tactics of the insurgents was to engage the police and administration through proxy, he observes.

Civilians significantly women were used as a proxy. Shilshi writes that many women, dressed in traditional funeral attire, were coerced to attend events such as the Ashti ritual ceremony of the Meitei community. That, Shilshi says, was done deliberately to provoke action from the district administration since such activities were tantamount to extending open support to members of the Underground, which is impermissible under the law. Thus, every Ashti ceremony of slain UG members ended in physical tussles between the police and public.

They engaged the police by placing women at the forefront of any pro-underground protest or processions to limit actions and to find convenient excuses to blame the police. This change in tactics threw up new challenges for us, writes Shilshi. Some groups particularly, the well-known United National Liberation Front and Peoples Liberation Army used women to their advantage, writes Shilshi.

In recent years, violence has considerably come down in Manipur. But as the author states, it is by no means the end of the problem nor an indication of complete decline in insurgent activities. Shilshi cautions that it could be a period of strategising. Quoting examples of countries like the Philippines, South Sudan and Nepal, he says that across the world, societies which have tasted the luxury of gun culture through armed conflict have found it extremely difficult to exit from it completely. Even after former rebels mainstreamed themselves, remnants threatened to resurface. We can ignore that at our own peril, warns Shilshi.

The writer is a freelance journalist based in Imphal

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Dissecting Manipurs anatomy of conflict - The Statesman

Anatomy of a win: Gov. Doug Burgum won big on Nov. 3, but still lost ground when compared to his 2016 totals – Grand Forks Herald

It was a commanding win but it also fell short of his 2016 victory by more than 10 points, when he won the governor's mansion with more than 75% of nearly 340,000 votes.

Burgum this year received 235,379 votes and Lenz received 90,763. In 2016, Burgum received 259,863 votes.

Precisely how Burgum came to lose those votes may not matter much in the coming session. He appears electorally untouchable a strong GOP incumbent in a deep-red state. But the shifts in his support from 2016 help sketch out exactly what's changed in the last four years, and give a glimpse at the political ground changing under North Dakota's feet.

Burgum saw his largest margins in western North Dakota, in and around the oil patch, and in rural regions throughout the state. In 30 counties, his share of the vote ran within 5 points either above or below of last election.

And its perhaps not surprising that his vote share was a little lower. As UND political scientist Mark Jendrysik put it, theres really nowhere to go from his 2016 performance but down from that commanding three-quarters of the vote.

But there are some key places where Burgum lost ground whether from the down-ballot effects of the presidential election, reactions to the pandemic or some other set of factors that pulled him back.

Democrats, for example, made gains in Burleigh County and along the I-29 corridor, where gubernatorial hopeful Shelley Lenz improved on the 2016 performance of Democrat Marvin Nelson. While Nelson had run at a dismal 19.4% of the statewide vote, Lenz picked more than 25%. Cass County was the epicenter for those gains, where Lenz was able to pick up a total 36.3% of the county's vote.

That's still an absolute beating for the Democratic-NPL but it appears to be an improvement over the previous cycle. In Cass County, Lenz outran Nelson by a remarkable 13.39% of the vote. In Burleigh, she outran him by nearly 10%, and in Grand Forks county, by nearly 8%.

In a sign of continuing realignment for the state party, Lenzs support was remarkably urban. Those three urban counties, together, accounted for 51.2% of Nelson's votes. On Tuesday, unofficial results showed they counted for more than 58.5% of Lenz's. That's the most since at least 2000, in a sign that the party's support just like its national counterpart is increasingly restricted to urban regions.

The reason that vote share surged is hard to tease out. Part of it could easily be the presidential election with votes for Democrats in both contests tracking upward in 2020. But in both years, the presidential candidate has outrun the North Dakota gubernatorial candidate.

Neither Burgum's campaign nor his office responded to a request to interview the governor for this report.

And while Burgum bled votes to Lenz, he also lost out to write-in candidates, who won significantly more ballots than in past cycles. Much of that is likely Michael Coachman, a conservative Air Force veteran who waged a write-in campaign on an aggressively limited-government platform.

The reporting requirements for write-in candidates make it hard to tell precisely how many write-in votes are Coachman's. This year's total 4.9% of the vote was far higher than before.

Coachman was far to Burgum's right on COVID-19, telling a crowd in October that he thinks Burgum's pandemic response went too far into North Dakotans' daily lives. Some had called him a bellwether for the strength of Burgum's political hand in the Legislature.

RELATED: Gubernatorial write-in candidate gaining support in western North Dakota

Multiple observers point out that a roughly 5% showing isn't nearly enough to matter as the next session convenes. But it does appear to be an indication that Burgum, choosing the middle road on his pandemic response urging masks, for example, but not requiring them could have cost himself votes both on his right and on his left.

"If it means something, who does it mean something to? Does it mean something to me?" said state Rep. Rick Becker, R-Bismarck. "Sure, because if Doug would have been a solid Republican candidate, then Coachman surely should have had less than one percent of the vote."

And like most observers, the Democratic-NPL Chairwoman Kylie Oversen points out that the item to watch in the coming session will be Burgums relationship with different factions within the Republican Party which will be tugged in different directions by responses to coronavirus, balancing the state budget and a new fight over the future of a deceased GOP candidates seat in District 8.

It's going to be an interesting dynamic to see how the Republican caucus fractures again, and how many factions come out of that break, she said.

Editor's note: This story was updated at noon Saturday, Nov. 14, to clarify that vote reporting requirements make it difficult to determine how many votes write-in candidates receive, under certain thresholds.

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Anatomy of a win: Gov. Doug Burgum won big on Nov. 3, but still lost ground when compared to his 2016 totals - Grand Forks Herald

‘Grey’s Anatomy’ And Katherine Heigl At Odds Again Over Scrapped Farewell Episode – HuffPost

Even in our wildest (Mc)dreams, no one ever expected Patrick Dempsey to return to Greys Anatomy after the controversy surrounding his exit.

But return he did in the closing moments of the two-hour Season 17 premiere, which saw Ellen Pompeo reuniting with her long-deceased onscreen husband in her dreams (at least its not a ghost, OK?) after collapsing.

On the heels of his appearance, many fans have been left wondering if Katherine Heigl might finally get her own swan song considering her rather abrupt departure from the show amid friction with creator Shonda Rhimes.

But, it turns out showrunner Krista Vernoff already penned a goodbye episode centered on Heigls character, Izzie Stevens, years ago that would have wrapped up her fan-favorite love story with Alex Karev (Justin Chambers).

In a Los Angeles Times interview published last week, Vernoff claimed that Heigl never showed up for filming.

We had planned to have her come back for an episode to really properly tie up Izzie and Alex, Vernoff told the outlet. I wrote that episode, and it was beautiful. The day before it was supposed to start prepping or shooting, I cant remember, we got a call that Katie wasnt coming. Just wasnt coming. Wasnt going to do it.

I dont know what was happening in her life, Vernoff added. I dont know what led to that decision. All I know is that the night before a thing is supposed to start shooting that is entirely centered on one character and the completion of her story arc, I got a phone call that she wasnt coming to do it.

Sources close to Heigl, however, have since refuted the story.

This account isnt true. Krista is mistaken, an unnamed source told Entertainment Weekly. Katherine was back in LA after parental leave (when she adopted her daughter) waiting to be called to set.

Heigl, one of the long-running medical dramas original cast members,remained on the ABC show from its debut in 2005 until 2010, when she exited midway through the sixth season.

At the time, Heigl rumors swirled that she was trying to break her contract on the series after repeatedly disparaging the show in the press, most notably when sheremoved her name from Emmy consideration in 2008 because she felt the material didnt warrant a nomination.

Reports at the time mirror Vernoffs claim that Heigl failed to show up for filming, while sources in the actors camp back then maintained that she was at home and ready to return to work.

While its highly unlikely that Heigl will ever walk the halls of Grey Sloan Memorial Hospital again, Vernoff said seeing an old cast member like Dempsey on set again was so moving and healing.

This show has been on for 17 seasons. Theres been some drama around some exits. And there have been enough years in the interim that everyone grows up; they grow up, they realize where they got things wrong, she told the Los Angeles Times. Theres always sort of two sides to every story. What it felt like was a homecoming.

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'Grey's Anatomy' And Katherine Heigl At Odds Again Over Scrapped Farewell Episode - HuffPost