Exelixis to Webcast Fireside Chats as Part of Upcoming Investor Conferences in September

On September 1, 2026 Exelixis, Inc. (Nasdaq: EXEL) reported that company management will participate in fireside chats at the following investor conferences in September:

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Wells Fargo 21st Annual Healthcare Conference: Exelixis is scheduled to present at 11:00 a.m. ET / 8:00 a.m. PT on Tuesday, September 8 in Boston.
Citi 2026 Biopharma Back to School Conference: Exelixis is scheduled to present at 8:40 a.m. ET / 5:40 a.m. PT on Wednesday, September 9 in New York City.
Morgan Stanley 24th Annual Global Healthcare Conference: Exelixis is scheduled to present at 11:30 a.m. ET / 8:30 a.m. PT on Tuesday, September 15 in New York City.
To access the webcast links, log onto www.exelixis.com and proceed to the Event Calendar page under the Investors & News heading. Replays will also be available at the same location for at least 30 days.

(Press release, Exelixis, SEP 1, 2026, View Source [SID1234670494])

BridgeBio to Participate in September Investor Conferences

On September 1, 2026 BridgeBio Pharma, Inc. (Nasdaq: BBIO) ("BridgeBio" or the "Company"), a commercial-stage, multi-product biopharmaceutical company focused on developing medicines for genetic conditions, reported that members of its management team will participate in fireside chats at the following healthcare investor conferences:

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21st Annual Wells Fargo Healthcare Conference, Boston, MA: Wednesday, September 9 at 1:30 pm EDT
2026 Cantor Global Healthcare Conference, New York, NY: Thursday, September 10 at 9:10 am EDT
Morgan Stanley 24th Annual Global Healthcare Conference, New York, NY: Tuesday, September 15 at 10:00 am EDT
Bernstein Insights Healthcare Leaders and Disruptors 2026, New York, NY: Wednesday, September 23 at 9:40am EDT

To access the live webcast of BridgeBio’s presentations, please visit the "Events and Presentations" page within the Investors section of the BridgeBio website at View Source A replay of the webcasts will be available on the BridgeBio website for 90 days following the event.

(Press release, BridgeBio, SEP 1, 2026, View Source [SID1234670493])

Domainex and Vipergen Partner to Accelerate Hit and Lead Discovery

On September 1, 2026 Domainex, a leading integrated drug discovery services partner, and Vipergen, a pioneering DNA-encoded library (DEL) screening company, reported a strategic collaboration to support lead discovery programmes across a range of disease targets.

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Through the collaboration, clients can now access Vipergen’s DEL screening capabilities alongside Domainex’s expertise in assay development, biophysics, medicinal chemistry, and integrated discovery services – providing a seamless, end-to-end solution from hit identification to validated leads.

A first client case study has already shown the partnership in action: Vipergen’s DEL screening platform identified novel molecular glue hits, and Domainex independently confirmed them through complementary biophysics and assay development work.

"This collaboration expands the range of hit and lead discovery solutions available to our clients by combining Vipergen’s unique DEL screening technology with Domainex’s established fragment-based and high-throughput screening (HTS) approaches, as well as our assay development, biophysics, and medicinal chemistry expertise. Together, we can help partners identify, validate, and progress high-quality starting points for their drug discovery programmes," said Dr Hayley French, CEO of Domainex.

"We are thrilled to partner with Domainex, whose broad and complementary drug discovery capabilities make them an ideal partner for Vipergen. This collaboration allows us to offer clients a truly integrated path from DEL screening hits to optimised leads – combining the unique advantages of our cell-based and in vitro DEL platforms with Domainex’s world-class assay and medicinal chemistry expertise," said Dr Nils Hansen, CEO of Vipergen.

Together, the two companies provide a complementary suite of technologies and expertise designed to streamline the transition from hit identification to validated lead series, helping accelerate early-stage drug discovery programmes.

(Press release, Vipergen, SEP 1, 2026, View Source [SID1234670492])

SCYNEXIS to Participate in Upcoming Investor Conferences

On September 1, 2026 SCYNEXIS, Inc. (Nasdaq: SCYX), a clinical-stage biotechnology company focused on developing innovative therapies for severe and difficult-to-treat diseases with significant unmet medical need, reported that the company will participate in the following investor conferences:

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12th Cantor Global Healthcare Conference in New York City
Fireside chat: Friday, September 11, 2026, at 9:45 a.m. ET.
H.C. Wainwright 28th Annual Global Investment Conference in New York City
1×1 investor meetings: September 14-16, 2026

A live webcast of the Cantor fireside chat will be available here. A replay will be available for 90 days following the event.

(Press release, Scynexis, SEP 1, 2026, View Source [SID1234670491])

Orca Bio to Present Clinical Data on TREGZI™ and Its Clinical Pipeline at the 14th Annual Meeting of the Society of Hematologic Oncology

On September 1, 2026 Orca Bio, a commercial-stage biotechnology company committed to transforming the lives of patients through high-precision cell therapy, reported that three clinical data and study updates have been accepted for presentation and publication at the 14th Annual Meeting of the Society of Hematologic Oncology from September 9 -12 in Houston, Texas.

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The presentations will include data on TREGZI, the company’s recently approved precision-engineered cell therapy for allogenic transplant in adults with hematologic malignancies, as well as an encore presentation on Orca Bio’s investigational allogeneic T-cell immunotherapy, Orca-Q .

"Our presence at the Society of Hematologic Oncology comes at an important time as it gives us the opportunity to share additional information on the profile of our recently approved therapy, TREGZI, to the hematology community," said Nate Fernhoff, Ph.D., co-founder and chief executive officer of Orca Bio. "As a company committed to redefining what’s possible in curative allogeneic cell therapy, we’re also pleased to share updates coming out of our clinical development program."

Details of the Orca Bio presentations follow:

Title: Clinical Overview of Infection Events with Orca-T vs Conventional Allogeneic Hematopoietic Stem Cell Transplantation in the Precision-T Phase 3 Study

Presentation ID: CT 594

Date and Time: September 9, 2026 at 6:25-7:55pm CT

Location: Hall B3, George R. Brown Convention Center

Title: Preliminary Safety and Efficacy of Myeloablative Orca-Q in Patients with Haploidentical Donors

Presentation ID: CT 931

Date and Time: September 9, 2026 at 6:25-7:55pm CT

Location: Hall B3, George R. Brown Convention Center

Title: SERENE-T: A Phase 2 Trial of Orca-T Following Reduced Intensity or Nonmyeloablative Conditioning in Patients with Acute Myeloid Leukemia or Myelodysplastic Syndrome

Accepted for publication in Clinical Lymphoma, Myeloma and Leukemia as part of the SOHO 2026 meeting proceedings supplement

Following the presentations, copies will be available on the Scientific Publications section of the Company’s website.

About TREGZI

TREGZI is the first-and-only FDA approved precision-cell therapy for allogeneic transplant in adults with hematologic malignancies to improve survival free of cGVHD. It is indicated for use in matched donor hematopoietic stem cell transplantation with myeloablative preparative regimen, for hematopoietic and immunologic reconstitution and to improve chronic graft-versus-host-disease-free survival, in the treatment of adults with hematological malignancies.

TREGZI is a personalized treatment manufactured for each individual patient using living cells from a matched donor. TREGZI uses hematopoietic stem and progenitor cells (HSPCs) to reconstitute the immune system, highly purified regulatory T cells (Tregs) to suppress GVHD and conventional T cells (Tcons) to accelerate immune reconstitution and produce graft-versus-leukemia (GVL) activity.

The FDA approval of TREGZI was based on the results of Precision-T, a randomized, open-label, multi-center study that evaluated the safety, efficacy and tolerability of TREGZI compared with conventional allogeneic hematopoietic stem cell transplant (alloHSCT).

About Orca-Q
Orca-Q is Orca Bio’s second-generation investigational allogeneic T-cell immunotherapy being evaluated 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, SEP 1, 2026, View Source;utm_medium=rss&utm_campaign=orca-bio-to-present-clinical-data-on-tregzi-and-its-clinical-pipeline-at-the-14th-annual-meeting-of-the-society-of-hematologic-oncology [SID1234670490])