Xilio Therapeutics Announces Clinical Trial Collaboration With Merck on Anti-CTLA-4 Monoclonal Antibody Program

On May 25, 2021 Xilio Therapeutics, a biotechnology company developing tumor-selective immuno-oncology therapies for patients with cancer, reported that it has entered into a clinical trial collaboration and supply agreement with Merck, known as MSD outside the United States and Canada, to evaluate XTX101, Xilio’s engineered tumor-selective Fc-enhanced, anti-CTLA-4 monoclonal antibody (mAb) product candidate, in combination with KEYTRUDA (pembrolizumab), Merck’s anti-PD-1 (programmed death receptor-1) therapy (Press release, Xilio Therapeutics, MAY 25, 2021, View Source [SID1234580570]). The planned clinical trial will be conducted by Xilio and is designed to evaluate the safety and efficacy of XTX101 as a monotherapy and in combination with KEYTRUDA in patients with solid tumors.

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"We believe tumor-selective immuno-oncology has significant potential to provide meaningful treatments to patients with a number of different cancers. The clinical benefit of targeting CTLA-4 as a treatment for cancer is well-established. However, treatment with the combination of an anti-CTLA-4 mAb and PD-1 checkpoint inhibitor has been associated with challenging toxicities, preventing patients from receiving effective doses of the anti-CTLA-4 antibody," said Marty Huber, M.D., chief medical officer of Xilio Therapeutics. "XTX101 is designed to be tumor-selective and based on data observed in preclinical studies, we believe it could be an ideal CTLA-4-targeting candidate to combine with checkpoint inhibitors like KEYTRUDA. We are pleased to partner with Merck to study this combination in an effort to improve therapeutic options for people with cancer."

XTX101 is a tumor-selective anti-CTLA-4 mAb designed to pinpoint the anti-CTLA-4 effect geographically within the tumor without off-tumor peripheral effects, potentially improving the therapeutic index and overcoming the potency and tolerability limitations of other anti-CTLA-4 antibodies. In preclinical studies, XTX101 has been well-tolerated and achieved robust tumor growth inhibition, including complete responses accompanied by tumor-selective immune activation. Xilio plans to submit an investigational new drug (IND) application for XTX101 to the U.S. Food and Drug Administration (FDA) in the second quarter of 2021. Subject to FDA clearance of the IND application, Xilio expects to promptly initiate a Phase 1 clinical trial evaluating XTX101 as a monotherapy and as a combination therapy with KEYTRUDA for the treatment of solid tumors.

Biodesix to Present at the William Blair 41st Annual Growth Stock Conference

On May 25, 2021 Biodesix, Inc. (Nasdaq: BDSX), a leading data-driven diagnostic solutions company with a focus in lung disease, reported Scott Hutton, Chief Executive Officer of Biodesix, will present at the William Blair 41st Annual Growth Stock Conference being held virtually June 1-3, 2021 (Press release, Biodesix, MAY 25, 2021, View Source [SID1234580569]).

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William Blair 41st Annual Growth Stock Conference
Date: Wednesday, June 2, 2021
Time: 2:00 PM CT

The presentation will be webcast live and available for replay under "News & Events" in the Investors section of the Company’s website at www.biodesix.com.

Blueprint Medicines to Present at Upcoming Investor Conferences

On May 25, 2021 Blueprint Medicines Corporation (NASDAQ: BPMC) reported its participation in the following upcoming investor conferences (Press release, Blueprint Medicines, MAY 25, 2021, View Source [SID1234580568]).

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Jefferies Virtual Healthcare Conference on Tuesday, June 1, 2021 at 4:30 p.m. ET.
Goldman Sachs 42nd Annual Global Healthcare Conference on Thursday, June 10, 2021 at 8:50 a.m. ET.
JMP Securities Life Sciences Conference on Wednesday, June 16, 2021 at 1:00 p.m. ET.
A live webcast of each presentation will be available by visiting the Investors & Media section of Blueprint Medicines’ website at View Source A replay of the webcasts will be archived on Blueprint Medicines’ website for 30 days following each presentation.

Verastem Oncology to Present at the 2021 Jefferies Virtual Healthcare Conference

On May 25, 2021 Verastem, Inc. (Nasdaq: VSTM) (also known as Verastem Oncology), a biopharmaceutical company committed to advancing new medicines for patients battling cancer, reported that the Company will present at the 2021 Jefferies Virtual Healthcare Conference on Tuesday, June 1, 2021 at 4:00 p.m. ET (Press release, Verastem, MAY 25, 2021, View Source [SID1234580567]).

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A live webcast of the presentation will be available on the investors section of the Company’s website at www.verastem.com. An archived presentation will be available for 30 days.

Autolus Therapeutics Announces an Additional Nature Publication for AUTO1

On May 25, 2021 Autolus Therapeutics plc (Nasdaq: AUTL), a clinical-stage biopharmaceutical company developing next-generation programmed T cell therapies, reported a publication in Nature Cancer that gives new insight into the mechanism of long-term durability of effect in acute lymphoblastic leukemia (ALL) patients treated with AUTO1 (Press release, Autolus, MAY 25, 2021, View Source [SID1234580566]).

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AUTO1 CAR T cells from pediatric ALL patients who still had CAR T cells detectable in the blood more than two years after their treatment were compared with patients who had lost their AUTO1 CAR T cells one to two months post treatment. The study shows that a subset of AUTO1 CAR T cells called Stem Cell Memory T-cells (TSCM) appear critical in both the initial anti-leukemic response and for long term immune surveillance. This suggests that this sub-group of AUTO1 CAR T cells contribute to the long-term durability of effect that AUTO1 has in these patients.

"AUTO1 has been designed to have an optimized interaction between its chimeric antigen receptor and the CD19 target on cancer cells," said Dr Martin Pule, Founder and Chief Scientific Officer of Autolus. "This means AUTO1 can efficiently deliver a kill and disengage rapidly like a normal T cell, leading to less exhaustion and less T cell differentiation. This unique property of AUTO1 potentially contributes to the enrichment and maintenance of this stem cell memory subset that appears to be critical to the long-term durability observed in pediatric ALL patients treated with AUTO1."