Ipsen delivers strong sales in the first quarter of 2026 and confirms its full-year guidance

On April 23, 2026 Ipsen reported its sales for the first quarter of 2026.

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(Press release, Ipsen, APR 23, 2026, View Source [SID1234665833])

Q1 2026 update

On April 23, 2026 Ipsen reported first quarter 2026 results.

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(Presentation, Ipsen, APR 23, 2026, View Source [SID1234665586])

Results Q1 2026

On April 23, 2026 Sanofi reported financial results of first quarter 2026.

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(Presentation, Sanofi, APR 23, 2026, View Source [SID1234665078])

Exicure Announces Co-Development Agreement with Adbiotech for Burixafor (GPC-100)

On April 23, 2026 Exicure, Inc. (Nasdaq: XCUR) reported that it has entered into a co-development agreement with Adbiotech Co., Ltd. (KOSDAQ: 179530), a Korea-based biotechnology company, to explore combination therapies based on Burixafor (GPC-100) across multiple therapeutic areas.

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The collaboration will focus on evaluating combination strategies involving Burixafor (GPC-100) in indications including sickle cell disease (SCD), acute myeloid leukemia (AML), and solid tumors.

Under the agreement, Adbiotech will conduct in vivo studies and support preclinical validation and translational research, while Exicure will provide Burixafor and lead clinical and regulatory strategy.

Burixafor successfully completed a Phase 2 clinical trial in multiple myeloma last year, providing a foundation for further evaluation in hematologic indications such as AML and SCD. Based on its clinical profile to date, Burixafor may have potential applicability in additional hematologic indications.

The parties intend to conduct in vivo validation studies and, subject to further agreement, may advance selected programs into IND-enabling studies and clinical trials. The parties also intend to secure funding to support the advancement of future clinical development.

Further details regarding development plans, budget, intellectual property, and commercialization will be determined in a subsequent definitive agreement.

A representative of Exicure commented, "This agreement represents an important step in expanding the evaluation of Burixafor in combination approaches across multiple indications."

(Press release, Exicure, APR 23, 2026, View Source [SID1234664745])

OSE Immunotherapeutics Announces Presentation of TEDOVA Phase 2 Topline Results of Tedopi® in Ovarian Cancer at the ASCO 2026 Meeting

On April 23, 2026 OSE Immunotherapeutics SA (ISIN: FR0012127173; Mnemo: OSE), a clinical-stage biotech company dedicated to developing first-in-class therapies in immuno-oncology and immuno-inflammation, reported that topline results from the TEDOVA Phase 2 international clinical trial of Tedopi in Ovarian Cancer sponsored by ARCAGY-GINECO have been selected for an oral presentation at the 2026 Annual Meeting of the American Society of Clinical Oncology (ASCO) (Free ASCO Whitepaper) in Chicago, Illinois, United States (May 29 – June 2, 2026).

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Alexandra Leary, MD, PhD, Deputy Head of the Department of Medical Oncology at Gustave Roussy (Paris, France), oncologist specialising in gynaecological cancers, Chair of the GINECO group and Lead Investigator of the TEDOVA Phase 2 clinical trial of Tedopi, will present topline results from the TEDOVA trial evaluating Tedopi as a maintenance treatment of ovarian cancer.

"The neo-epitope-based vaccine OSE-2101 with or without pembrolizumab versus best supportive care as maintenance in platinum-sensitive recurrent ovarian cancer patients with controlled disease after platinum-based chemotherapy: The academic randomized TEDOVA/GINECO-OV244b/ENGOT-ov58 trial"

Rapid Oral Abstract
Session: Gynecologic Cancer – Subtrack: Ovarian Cancer
Abstract 5510
Room: E450
May 30, 2026, 8:06-8:12am CDT (3:06-3:12pm EST)
TEDOVA is a three-arm Phase 2 study evaluating Tedopi as a maintenance treatment, alone or in combination with anti-PD1 immune checkpoint inhibitor Keytruda (pembrolizumab), versus best supportive care in 185 patients in platinum-sensitive recurrent ovarian cancer with controlled disease after platinum-based chemotherapy who have already received both bevacizumab and a PARP (Poly ADP-Ribose Polymerase) inhibitor. The primary endpoint is the Progression Free Survival (PFS) of the maintenance of Tedopi, with a PD1 inhibitor, after platinum-based chemotherapy in relapsed ovarian cancer.
(NCT04713514).

(Press release, OSE Immunotherapeutics, APR 23, 2026, View Source [SID1234664744])