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Intellectia

MOLN News

Molecular Partners Initiates DLL3-Targeting Therapy Study

2h agoYahoo Finance

Molecular Partners and Orano Med Initiate DLL3-Targeting Therapy Clinical Trial

2h agoNewsfilter

Molecular Partners Announces Clinical Trial Progress

May 30 2026Newsfilter

Molecular Partners Q1 Earnings Miss Expectations

May 12 2026seekingalpha

Molecular Partners to Present at Scientific Conferences

May 04 2026Newsfilter

Positive Phase 1 Data for MP0317 in Cancer Treatment

May 01 2026Newsfilter

Molecular Partners Unveils First Logic-Gated Switch-DARPin T Cell Engager Candidate

Apr 19 2026Newsfilter

Molecular Partners Reports FY 2025 Financial Results with Significant Losses

Mar 12 2026seekingalpha

MOLN Events

05/31 16:30
Molecular Partners to Present MP0712 Trial Progress at 2026 ASCO Meeting
Molecular Partners announced it will hold trial-in-progress poster presentations on the Phase 1/2a study of its lead targeted alpha radiotherapy candidate MP0712 at the 2026 American Society of Clinical Oncology, ASCO, Annual Meeting and the Society of Nuclear Medicine and Molecular Imaging, SNMMI, Annual Meeting. ASCO takes place May 29-June 2 in Chicago, and SNMMI May 30-June 2 in Los Angeles. The US multicenter Phase 1/2a study of MP0712 is actively recruiting patients with dosing ongoing in the first cohort. The Phase 1/2a study objectives are to assess safety and determine a recommended Phase 2 dose for MP0712. Molecular Partners expects to share initial clinical data from this study in 2026.
05/01 07:10
Molecular Partners Publishes MP0317 Clinical Data
Molecular Partners announced the publication of Phase 1 clinical data in Nature Cancer demonstrating the potential of the tumor-localized CD40 agonist, MP0317, to modulate the tumor microenvironment. MP0317 is designed to activate immune cells specifically within the TME by anchoring to fibroblast activation protein, which is expressed in high amounts in the stroma of various solid tumors. This tumor-localized approach has the potential to deliver greater efficacy with fewer side effects compared to systemic CD40-targeting therapies. The peer-reviewed paper published by Steehgs et al., entitled "Tumor-localized CD40 agonism with MP0317, a FAPxCD40 DARPin, reprograms the tumor microenvironment - results of a Phase 1 monotherapy study", reports the positive results from the completed Phase 1 dose escalation study of MP0317. The comprehensive biomarker data confirm proof-of-mechanism for MP0317, including tumor-localized activation of the CD40 pathway and evidence of TME remodeling in patients with advanced solid tumors. MP0317 displayed a favorable safety profile up to the highest tested dose and serum pharmacokinetics confirmed suitability for dosing either weekly or every three weeks. Of the 46 patients in the study, one patient achieved an unconfirmed partial response and 14 patients stable disease in this heterogeneous population with advanced diseases. Data were presented at the 2024 Annual Meetings of the American Society of Clinical Oncology and of the Society for Immunotherapy of Cancer.
04/19 13:00
Molecular Partners Presents New Data on MP0632 at AACR Meeting
Molecular Partners announced the presentation of new preclinical data across three posters at the American Association for Cancer Research, AACR, Annual Meeting 2026. The first poster outlines preclinical data supporting proof-of-concept for MP0632, a logic-gated Switch-DARPin CD3 T cell engager with CD2 co-stimulation designed to selectively kill cells co-expressing mesothelin and epithelial cell adhesion molecule. MP0632 leads to regression of established tumors expressing both EpCAM and MSLN, with minimal impact on tumors expressing only one antigen, indicating a favorable therapeutic window. In addition, the Switch-DARPin candidate allowed for safe use of potent costimulation for efficient tumor cell killing with low cytokine release profile. The data support MP0632's potential as clinical lead candidate for the treatment of ovarian cancer and other MSLN- and EpCAM-positive solid tumors. The second poster presents a computational workflow to identify and prioritize tumor-associated antigen pairs for improved tumor-selectivity and safety in support of designing novel Switch-DARPin candidates, such as MP0632. This scalable, data-driven platform provides a strong foundation for the discovery of next-generation multispecific immunotherapies. The third poster outlines the molecular characteristics of MP0712, the Company's first 212Pb-based Radio-DARPin candidate, with high affinity binding to DLL3 and optimized half-life extended properties.
02/26 05:50
Molecular Partners Enters Agreement with Eckert & Ziegler for Radio-DARPin Development
Molecular Partners announced it has entered into an agreement with Eckert & Ziegler to enable the development and manufacturing of Radio-DARPin therapeutics. Under the non-exclusive agreement, Eckert & Ziegler will support Molecular Partners with a range of services covering development activities for Radio-DARPins with Actinium-225 and Lutetium-177 payloads. The development agreement will leverage Eckert & Ziegler's laboratories, including its newly established Alpha Laboratory in Berlin, Germany, dedicated exclusively to work with alpha emitters.

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