Rigel Announces Poster Presentation at the Upcoming 2023 American Society of Clinical Oncology Annual Meeting

On June 1, 2023 Rigel Pharmaceuticals, Inc. (Nasdaq: RIGL) reported an upcoming poster presentation highlighting the Company’s IRAK1/4 program at the 2023 American Society of Clinical Oncology (ASCO) (Free ASCO Whitepaper) Annual Meeting being held June 2-6, 2023, in Chicago, IL, and virtually (Press release, Rigel, JUN 1, 2023, View Source [SID1234632355]).

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Rigel continues to advance the open-label, Phase 1b clinical trial of R2891, an investigational, potent, and selective IRAK1/4 inhibitor, in patients with lower-risk myeloid dysplastic syndrome (LR-MDS) who are refractory/resistant to prior therapies. Rigel has completed enrollment of the first cohort of the trial and enrollment of the second cohort is underway.

Poster Presentation Details:

Abstract #: TPS7085
Title: Phase 1b Clinical Study of IRAK 1/4 Inhibition for Low-Risk Myelodysplastic Syndromes Refractory/Resistant to Prior Therapies
Lead Author: Guillermo Garcia-Manero, M.D., Professor, Chief Section MDS, Deputy Chair Translational Medicine, Leukemia, University of Texas MD Anderson Cancer Center
Session Name: Hematologic Malignancies – Leukemia, Myelodysplastic Syndromes, and Allotransplant
Date: June 5, 2023
Presentation Time: 8:00-11:00 AM CDT
Location: Hall A

The conference abstract can be accessed here.

To learn more about Rigel Pharmaceuticals and the Company’s clinical and commercial hematology/oncology portfolio visit booth #20134 during ASCO (Free ASCO Whitepaper).

About R289
R289 is a prodrug of R8351, an IRAK1/4 dual inhibitor, which has been shown in preclinical studies to block inflammatory cytokine production in response to toll-like receptor (TLR) and interleukin-1 receptor (IL-1R) family signaling. TLRs and IL-1Rs play a critical role in the innate immune response and dysregulation of these pathways can lead to various inflammatory conditions. Chronic stimulation of both these receptor systems is thought to cause the pro-inflammatory environment in the bone marrow responsible for persistent cytopenias in lower-risk MDS patients.

Replimune to Present at the Jefferies Global Healthcare Conference

On June 1, 2023 Replimune Group, Inc. (NASDAQ: REPL), a clinical stage biotechnology company pioneering the development of a novel portfolio of tumor-directed oncolytic immunotherapies, reported that members from the Replimune management team will present in a fireside chat at the Jefferies Global Healthcare Conference on Thursday, June 8, 2023 at 1:00 PM ET at the Marriot Marquis in New York NY (Press release, Replimune, JUN 1, 2023, View Source [SID1234632354]).

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Corporate presentation

On June 1, 2023 Prelude therapeutics presented its corporate presentation (Presentation, Prelude Therapeutics, JUN 1, 2023, View Source [SID1234632353]).

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Philogen Announces Clinical Trial Collaboration with MSD

On June 1, 2023 Philogen S.p.A., a clinical-stage biotechnology company focused on the development of innovative medicines based on tumor-targeting antibodies and small molecule ligands, reported that it has entered into a Clinical Trial Collaboration and Supply Agreement with MSD (Merck & Co., Inc., Rahway, NJ, USA) (Press release, Philogen, JUN 1, 2023, View Source [SID1234632352]). Under the terms of the supply agreement, MSD provides their anti-PD-1 therapy, KEYTRUDA (pembrolizumab), to be evaluated in combination with Philogen’s immunocytokines L19IL2, L19TNF, and Nidlegy in a randomized Phase II clinical trial. The study provides an opportunity to explore the combination of immunocytokines and PD-1 blockade in stage III and IV unresectable melanoma patients who failed prior checkpoint inhibitor therapies.

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Nidlegy is also investigated in two Phase III randomized clinical trials for the treatment of stage III B/C melanoma in Europe and in the United States, as well as in two Phase II clinical trials in High-Risk Basal Cell Carcinoma and other non-melanoma skin cancers.

Dario Neri, CEO and CSO of Philogen, commented: "KEYTRUDA has shown impressive response rates and long-term benefits for a substantial number of patients with advanced melanoma. However, only a minor proportion of patients who fail checkpoint inhibitors typically benefit from a subsequent re-challenge with single-agent PD-1 blockade. Clinical experience with intralesional recombinant IL2 has shown encouraging response rates when combined with systemic anti-PD-1 antibodies in advanced melanoma patients who progressed on or are resistant to checkpoint inhibitors. This provides a strong rationale to combine Nidlegy (L19IL2 + L19TNF) with KEYTRUDA in this setting, and we are pleased to partner with MSD, a global leader in immuno-oncology, to explore this opportunity."

KEYTRUDA is a registered trademark of Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA. Nidlegy is a registered trademark of Philogen S.p.A. of La Lizza 7, 53100 Siena, ITALY

Developing Transformational Immunotherapies for Cancer

On June 1, 2023 PDS Biotechnology presented its corporate presentation (Presentation, PDS Biotechnology, JUN 1, 2023, View Source [SID1234632351]).

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