Orca Bio to Present New Clinical Data on Its High-Precision Cell Therapies at the 67th American Society of Hematology Annual Meeting

On November 3, 2025 Orca Bio, a late-stage biotechnology company committed to transforming the lives of patients through high-precision cell therapy, reported that new clinical data will be presented in three oral and three poster sessions at the American Society of Hematology (ASH) (Free ASH Whitepaper) Annual Meeting from December 6-9 in Orlando, FL. The presentations will span its pipeline of investigational allogeneic T-cell immunotherapies for the treatment of multiple hematological malignancies including Orca-T, Orca-Q and the Orca-T and allogeneic CAR-T combination therapy, OrCAR-T.

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"Our ongoing clinical evaluation of our pipeline across diverse patient populations, conditioning regimens and donor types underscores our commitment to advancing care for people with blood cancer," said Nate Fernhoff, Ph.D., co-founder and chief executive officer of Orca Bio. "We look forward to presenting new and expanded evidence from the pivotal Phase 3 study of our lead T-cell immunotherapy, Orca-T, along with data highlighting the potential of our next-generation candidate, Orca-Q, to enable treatment without GvHD prophylaxis. Overall, these findings mark meaningful progress toward our goal of delivering our high-precision approach to more patients who may benefit."

The ASH (Free ASH Whitepaper) abstracts are now available at www.hematology.org. Details of the Orca Bio oral and poster presentations follow:

Oral Session: 721. Allogeneic Transplantation: Conditioning Regimens, Engraftment, and Acute Toxicities: Improving Outcomes by Decreasing Transplant-Related Complications

Title: Allogeneic HSC and Regulatory T cell (Orca-T) Engineered Cell Therapy Following Reduced Intensity Conditioning: Results of a Single Center Phase 1 Study

Abstract Number: 111

Date and Time: December 6, 2025 at 10:00 AM EST

Location: OCCC – Chapin Theater (320)

Oral Session: 732. Allogeneic Transplantation: Disease Response and Comparative Treatment Studies: Biologic Predictors and Novel Platforms Integrating CAR T with Transplant

Title: Superior Efficacy and Persistence of Orca-T-Allogeneic CAR19/22 Versus Autologous CAR19/22 in High-Risk Adult B-ALL

Abstract Number: 514

Date and Time: December 7, 2025 at 10:15 AM EST

Location: OCCC – Chapin Theater (320)

Oral Session: 722. Allogeneic Transplantation: Acute and Chronic GVHD and Immune Reconstitution: GVHD Prevention: Post-transplant cyclophosphamide and beyond

Title: Preliminary Safety and Efficacy of Myeloablative Orca-Q with Tacrolimus or without GVHD Prophylaxis for Treatment of Advanced Hematologic Malignancies

Abstract Number: 932

Date and Time: December 8, 2025 at 3:00 PM EST

Location: OCCC – W331

Poster Session: 722. Allogeneic Transplantation: Acute and Chronic GVHD and Immune Reconstitution: Poster I

Title: Orca-T Improves cGVHD-free Survival in Patients with a Broad Range of Demographic and Clinical Variables: Results of Randomized, Phase 3 Trial

Abstract Number: 2477

Date and Time: December 6, 2025 at 5:30 PM – 7:30 PM EST

Location: OCCC – West Halls B3-B4

Poster Session: 722. Allogeneic Transplantation: Acute and Chronic GVHD and Immune Reconstitution: Poster I

Title: Orca-T Demonstrates Favorable Quality of Life and Healthcare Resource Use Compared to Standard AlloHSCT plus Tac/MTX for GVHD Prevention in a Randomized Phase 3 Clinical Trial (Precision-T)

Abstract Number: 2473

Date and Time: December 6, 2025 at 5:30 PM – 7:30 PM EST

Location: OCCC – West Halls B3-B4

Poster Session: 722. Allogeneic Transplantation: Acute and Chronic GVHD

and Immune Reconstitution: Poster III

Title: Observational Comparison of Orca-T to Registry-Based Post-Transplant Cyclophosphamide Patients using Matched Unrelated Donor

Abstract Number: 6029

Date and Time: December 8, 2025 at 6:00 PM – 8:00 PM EST

Location: OCCC – West Halls B3-B4

About Orca-T
Orca-T is an investigational allogeneic T-cell immunotherapy under evaluation for the treatment of multiple hematologic malignancies including acute leukemias and myelodysplastic syndromes. Orca-T is composed of highly purified regulatory T-cells, hematopoietic stem cells and conventional T-cells derived from either related or unrelated matched donors. Orca-T has received Regenerative Medicine Advanced Therapy (RMAT) and Orphan Drug Designation for the prevention of graft versus host disease or death in patients eligible for hematopoietic stem cell transplant from the U.S. Food and Drug Administration (FDA). The Biologics License Application (BLA) for Orca-T is currently under Priority Review with the FDA with a PDUFA target action date of April 6, 2026.

About Orca-Q
Orca-Q is Orca Bio’s second-generation investigational allogeneic T-cell immunotherapy under evaluation in clinical trials for the treatment of multiple hematologic malignancies, including in patients with haploidentical and mismatched donors. Orca-Q is a proprietary composition of stem cells combined with specific T-cell subsets derived from healthy donors and engineered by Orca Bio’s high-precision platform.

(Press release, Orca Bio, NOV 3, 2025, View Source;utm_medium=rss&utm_campaign=orca-bio-to-present-new-clinical-data-on-its-high-precision-cell-therapies-at-the-67th-american-society-of-hematology-annual-meeting [SID1234659271])

Olema Oncology to Participate in Upcoming Investor Conferences

On November 3, 2025 Olema Pharmaceuticals, Inc. ("Olema", or "Olema Oncology", Nasdaq: OLMA), a clinical-stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted therapies for breast cancer and beyond, reported that the Company will participate in the following upcoming investor conferences:

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Guggenheim 2nd Annual Healthcare Innovation Conference
Date and Time: November 10, 2025 at 10:30 a.m. ET
Format: Fireside Chat
Location: Boston, MA

UBS Global Healthcare Conference 2025
Date and Time: November 12, 2025 at 8:00 a.m. ET
Format: Presentation
Location: Palm Beach, FL

2025 Jefferies London Healthcare Conference
Date and Time: November 19, 2025 at 9:00 a.m. GMT / 4:00 a.m. ET
Format: Fireside Chat
Location: London

Live webcasts and recordings of these presentations will be available, as permitted by the event host, in the Events and Presentations section of Olema’s investor relations website at ir.olema.com.

(Press release, Olema Oncology, NOV 3, 2025, View Source [SID1234659270])

Nurix Therapeutics Announces Presentations at the 67th American Society of Hematology (ASH) Annual Meeting

On November 3, 2025 Nurix Therapeutics, Inc. (Nasdaq: NRIX), a clinical-stage biopharmaceutical company focused on the discovery, development and commercialization of targeted protein degradation medicines in oncology and autoimmune disease, reported that updated clinical data from the NX-5948-301 Phase 1a/1b clinical trial have been selected for presentation at the 67th American Society of Hematology (ASH) (Free ASH Whitepaper) Annual Meeting and Exposition, taking place December 6 – 9, 2025, in Orlando, Florida. The data will be featured in two presentations: an oral presentation with new results in patients with relapsed or refractory chronic lymphocytic leukemia (CLL) and a poster presentation with updated results in patients with Waldenström macroglobulinemia.

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In addition to these clinical presentations, Nurix and its collaborators will also present new mechanistic insights into resistance to Bruton’s tyrosine kinase (BTK) targeted therapies at a separate ASH (Free ASH Whitepaper) poster session, highlighting discoveries that expand the understanding of BTK biology.

Oral Presentation Details:

Title: Bexobrutideg (NX-5948), a Novel Bruton’s Tyrosine Kinase (BTK) Degrader, Demonstrates Rapid and Durable Clinical Responses in Relapsed / Refractory Chronic Lymphocytic Leukemia (CLL): New and Updated Findings from an Ongoing Phase 1a/b Trial
Presenter: Zulfa Omer, M.D., Assistant Professor Internal Medicine, College of Medicine, University of Cincinnati, Cincinnati, OH, USA
Session Name: 642. Chronic Lymphocytic Leukemia: Clinical and Epidemiological: Treatment of CLL in Relapse and in Richter Transformation
Abstract #: 86
Session Date and Time: Saturday, December 6, 2025, 9:30 a.m. – 11:00 a.m. ET
Presentation Time: 9:45 a.m. – 10:00 a.m. ET
Room: Orange County Convention Center – W224ABEF

Poster Presentation Details

Title: Bexobrutideg (NX-5948), a Novel Bruton’s Tyrosine Kinase (BTK) Degrader, Shows High Clinical Activity and Tolerable Safety in Patients with Waldenström Macroglobulinemia: Updated Results from an Ongoing Phase 1a/b Study
Presenter: Scott Huntington M.D., MPH, Associate Professor of Internal Medicine (Hematology), Yale School of Medicine
Session Name: 623: Mantle Cell, Follicular, Waldenstrom’s, and Other Indolent B Cell Lymphomas: Clinical and Epidemiological: Poster III
Abstract # 5359
Session Date and Time: Monday, December 8, 2025, 6:00 p.m. – 8:00 p.m. ET
Location: Orange County Convention Center – West Halls BЗ – B4

Title: Molecular and Structural Basis of Pan-Resistance to BTK Targeting Therapies via BTK A428D Mutation
Presenter: Quinlan Sievers, M.D., Ph.D. Memorial Sloan Kettering Cancer Center, New York, NY
Session Name: 641:Chronic Lymphocytic Leukemia: Basic and Translational Poster I
Abstract # 2102
Session Date and Time: Saturday, December 6, 2025, 5:30 p.m. – 7:30 p.m. ET
Location: Orange County Convention Center – West Halls BЗ – B4

About Bexobrutideg (NX-5948)
Bexobrutideg is an investigational, orally bioavailable, brain penetrant, small molecule degrader of BTK currently being evaluated in the DAYBreak CLL-201 clinical trial (NCT07221500), a pivotal single-arm Phase 2 study of bexobrutideg in patients with relapsed or refractory chronic lymphocytic leukemia. Nurix also continues enrollment in the NX-5948-301 Phase 1a/1b clinical trial (NCT05131022) of bexobrutideg in patients with relapsed or refractory B cell malignancies. Additional information on the ongoing clinical trials can be accessed at clinicaltrials.gov.

(Press release, Nurix Therapeutics, NOV 3, 2025, View Source [SID1234659269])

NANOBIOTIX to Participate in Investor Conferences the Week of November 10th

On November 3, 2025 NANOBIOTIX (Euronext: NANO – NASDAQ: NBTX – the "Company"), a late-clinical stage biotechnology company pioneering nanotherapeutic approaches to expand treatment possibilities for patients with cancer and other major diseases, reported that Company management will participate in fireside chats at following conferences:

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UBS Global Healthcare Conference
Date: Monday, November 10, 2025
Time: 5pm ET / 11pm CET
Location: Palm Beach Gardens, FL
Presenter: Bart van Rhijn, Chief Financial & Business Officer of Nanobiotix

Guggenheim’s Annual Healthcare Innovation Conference
Date: Monday, November 10, 2025
Time: 4:30pm ET / 10:30pm CET
Location: Boston, MA
Presenter: Laurent Levy, Chief Executive Officer of Nanobiotix
Webcast link: Click here

Stifel Healthcare Conference
Date: Thursday, November 13, 2025
Time: 8am ET / 2pm CET
Location: New York, NY
Presenters: Laurent Levy, Chief Executive Officer of Nanobiotix and Bart van Rhijn, Chief Financial & Business Officer of Nanobiotix

The recorded fireside chats will be webcast live from the events page of the Investors section of the Company’s website. Replay of the webcast will be available following the event.

(Press release, Nanobiotix, NOV 3, 2025, View Source [SID1234659268])

MaaT Pharma Announces Positive Phase 3 Results Evaluating Xervyteg® (MaaT013) in Acute Graft-versus-Host Disease Selected for Oral Presentation at ASH Congress 2025

On November 3, 2025 MaaT Pharma (EURONEXT: MAAT – the "Company"), a clinical-stage biotechnology company and a leader in the development of Microbiome Ecosystem TherapiesTM (MET) dedicated to enhancing survival for patients with cancer through immune modulation, reported that results from its pivotal Phase 3 ARES trial evaluating Xervyteg (MaaT013) in patients with gastrointestinal acute Graft-versus-Host Disease refractory to steroids and refractory or intolerant to ruxolitinib (SR GI-aGvHD) will be presented in an oral session at the 67th American Society of Hematology (ASH) (Free ASH Whitepaper) Annual Meeting and Exposition that will take place December 6-9, 2025, in Orlando, Florida, USA. This marks the ninth consecutive year that MaaT Pharma’s clinical data has been selected for presentation at ASH (Free ASH Whitepaper) annual meeting, and the first time the Company will present its Phase 3 results at a medical congress.

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"For the ninth consecutive year, MaaT Pharma is proud to present data at ASH (Free ASH Whitepaper), reaffirming our position as the undisputed leader in microbiotherapy for hematology-oncology. The ARES study demonstrated a clinically meaningful and durable benefit in patients with gastrointestinal aGvHD, further validating our approach and its potential to redefine the standard of care in this high unmet need," said Hervé Affagard, CEO and co-founder of MaaT Pharma.

The ARES trial met its primary endpoint and topline results were announced in January 2025. At the upcoming ASH (Free ASH Whitepaper) annual meeting, the Company will detail secondary endpoints, such as GI-ORR at D56 and Month 3 (M3), and some safety data. Final results, including 1-year overall survival, are expected by the end of 2025.

In the single-arm ARES study, 66 adult patients with GI-aGvHD refractory to steroids and refractory to ruxolitinib were treated with Xervyteg (MaaT013) as third-line treatment across 50 European sites in 6 countries (Austria, Belgium, France, Germany, Italy and Spain). The vast majority of patients included in the study (91%, n=60) presented with severe gastrointestinal aGvHD, classified as grade III (58%, n=38) or grade IV (33%, n=22). Among them, 86% (n=57) were steroid-resistant and 14% (n=9) steroid-dependent; all were refractory to ruxolitinib.

Efficacy data to be presented at the ASH (Free ASH Whitepaper) annual meeting is summarized below (see here for full abstract) – (up to the data cut-off of November 11, 2024):

GI-Overall Response Rate at Day 28 occurred in 41/66 patients (62%) and prevalently consisted of complete response (CR) (25/66 patients, 38%) and very good partial response (VGPR) (13/66 patients, 20%).
Overall Response Rate (all organs) at Day 28 occurred in 42/66 patients (64%) patients and was similarly driven by high rates of CR (24/66 patients, 36%) and VGPR (12/66 patients, 18%).
GI-ORR at Day 56 was maintained in 49% (31/ 63 patients) and prevalently consisted of CR (37%)
GI-ORR at 3 months was 44% (27/ 62 patients), with a prevalence of GI-CR (36%).
Average duration of response was 6.4 months
Probability of overall survival (OS) at 12 months:
The estimated OS was 54% with a median follow-up of 140.5 days (median survival not reached).
The estimated OS was significantly higher in patients who had a GI response at Day 28 than those who did not respond (67% vs 28% respectively, p <0.0001), demonstrating Xervyteg (MaaT013)’s significant survival benefit in refractory GI-aGvHD.
The median OS of responders was not reached while it was 54 days in non-responders.
Xervyteg (MaaT013) is currently under review by the European Medicines Agency (EMA) following the submission of a Marketing Authorization Application in June 2025, with a decision anticipated in the second half of 2026.

Details of the Oral Presentation:

Title: MaaT013 for ruxolitinib-refractory acute graft-versus-host disease with gastrointestinal involvement: Results from the ARES phase III trial
Publication Number: 817
Presenting Author: Prof. Malard, MD, hematology professor at Saint-Antoine Hospital and Sorbonne University, lead investigator for the Phase 3 ARES trial
Session Date: December 8, 2025
Presentation Time: 10:30 AM – 10:45 AM
Session Name: 722. Allogeneic Transplantation: Acute and Chronic GVHD and Immune Reconstitution: Clinical and Translational Insights
Room: OCCC – Sunburst Room (W340)
Upcoming investor and medical conferences participation

November 5-9, 2025 – 40th SITC (Free SITC Whitepaper) annual meeting in National Harbor, MD, USA
November 19-21, 2025 – SFGM-TC annual meeting in Geneva, Switzerland
November 25, 2025 – Investir Day event, Paris, France
December 6-9, 2025 – 67th ASH (Free ASH Whitepaper) annual meeting in Orlando, FL, USA

(Press release, MaaT Pharma, NOV 3, 2025, View Source [SID1234659267])