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Molecular Partners Showcases Bispecific Radio-DARPins at Gordon Research Conference

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Molecular Partners (SIX: MOLN; NASDAQ: MOLN) is presenting new data on its bispecific and multispecific Radio-DARPins at the Gordon Research Conference on Radionuclide Theranostics for the Management of Cancer in Newry, Maine, on July 15, 2026. The talk, given by SVP Targeted Radio Therapeutics Daniel Steiner, focuses on designing DARPins that align binding properties, half-life, and biodistribution with tumor and disease biology to overcome target limitations in radioligand therapy.

The company highlights mono-targeting and multispecific formats, including bispecific constructs and 2-in-1 DuoDARPins, intended to address tumor heterogeneity and co-expressed tumor targets. Lead candidate MP0712 (DLL3; with Orano Med) is in a US Phase 1/2a trial, while MP0726 (MSLN) is progressing toward first human imaging and a third Radio-DARPin program is planned for 2026.

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Positive

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Negative

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News Market Reaction – MOLN

-2.25%
-2.25% Session close to close

In the Jul 15 session, MOLN declined 2.25%, reflecting a moderate negative market reaction.

Data tracked by StockTitan Argus on the day of publication.

Market Context

Historical news has produced modest, mixed price responses, so investors may focus instead on how th...
Analysis

Historical news has produced modest, mixed price responses, so investors may focus instead on how these multispecific programs progress toward later-stage data.

Key Figures

Trial phase: Phase 1/2a
1 metrics
Trial phase Phase 1/2a Multicenter US trial of lead Radio-DARPin candidate MP0712

Historical Context

5 past events · Latest: Jul 06 (Positive)
Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Jul 06 Pipeline update Positive +0.5% Update on clinical progress across expanding Radio-DARPin pipeline, including MP0712.
Jul 02 Clinical trial start Positive +1.3% First patients dosed in US Phase 1/2a trial of DLL3 Radio-DARPin MP0712.
May 26 Conference participation Neutral -0.3% Announcement of participation in TD Cowen’s 7th Annual Oncology Innovation Summit.
May 12 Earnings and pipeline Neutral -1.0% Q1 2026 financial results with clinical studies initiated for MP0712 and MP0317.
May 04 Conference presentations Neutral +3.9% Multiple upcoming oral presentations on lead Radio-DARPin candidate MP0712 in May 2026.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Recent Molecular Partners news has generally been followed by modest, mixed share reactions, with several pipeline updates coinciding with small gains.

Key Terms

radioligand therapy, radionuclide theranostics, phase 1/2a, dosimetry
4 terms
radioligand therapy medical
"highlights its approaches to overcoming target limitations in radioligand therapy (RLT)"
A treatment that uses a small molecule or antibody designed to seek out specific cells and deliver a tiny dose of radiation directly to them, like a guided missile carrying a limited explosive to a particular target rather than carpeting an area. Investors care because successful radioligand therapies can become high-value prescription products with clear market niches, regulatory hurdles, and reimbursement decisions that strongly affect a developer’s revenue and risk profile.
radionuclide theranostics medical
"Gordon Research Conference Radionuclide Theranostics for the Management of Cancer"
A medical approach that uses tiny radioactive drugs both to find disease with imaging and to treat it by delivering radiation directly to the affected tissue. Think of it like a homing beacon that first pinpoints a tumor and then carries a therapeutic payload to the same spot. It matters to investors because it creates new product, manufacturing, regulatory and reimbursement pathways that can drive clinical adoption, company value, and market opportunity in oncology and other specialties.
phase 1/2a medical
"MP0712, co-developed with Orano Med and targeting delta-like ligand 3 (DLL3), is in a multicenter US Phase 1/2a trial"
Phase 1/2a is an early stage in testing new medicines or treatments, combining two steps into one process. It helps researchers quickly assess whether a treatment is safe and shows signs of working, while also gathering initial information on the best dosage. For investors, this stage indicates how close a potential new therapy is to becoming available and its initial safety profile.
dosimetry medical
"building on the successful generation of first imaging and dosimetry data from a compassionate care program"
Dosimetry is the measurement and calculation of how much ionizing radiation is absorbed by people, tissues, or devices, similar to a thermostat tracking temperature in different rooms to know where and how much heat is present. Investors should care because accurate dosimetry underpins safety, treatment effectiveness, regulatory approval, and liability for products and services that use radiation—affecting market access, costs, and commercial risk.

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  • Developing bispecific Radio-DARPins to engage multiple tumor targets simultaneously, improving precision and therapeutic efficacy

  • Presentation outlines Radio-DARPins’ ability to match target and disease biology for improved outcomes

ZURICH-SCHLIEREN, Switzerland and CONCORD, Mass., July 15, 2026 (GLOBE NEWSWIRE) -- Molecular Partners AG (SIX: MOLN; NASDAQ: MOLN), a clinical-stage biotech company developing a novel class of custom-built protein drugs known as DARPin therapeutics (“Molecular Partners” or the “Company”), today highlights its approaches to overcoming target limitations in radioligand therapy (RLT) through Radio-DARPins, in a presentation at the Gordon Research Conference Radionuclide Theranostics for the Management of Cancer in Newry, Maine, US.

Title: Appropriate Targets for RLT? High selectivity vs high expression
Presenter: Daniel Steiner, Ph.D.
Time: Wednesday July 15 at 11:10-11:30 ET

The presentation outlines the ability of DARPins to match the biological characteristics of both the target and the disease, by optimizing their binding properties, systemic half-life, and biodistribution. To address tumor heterogeneity, Molecular Partners is also developing multispecific Radio-DARPins that can engage multiple tumor targets simultaneously, improving precision and therapeutic efficacy.

"Our multispecific Radio-DARPin approaches reflect Molecular Partners’ ambition to push the boundaries of radiotheranostics and address the complexity and heterogeneity of cancer. By combining the versatility of DARPins with our deep expertise in designing multispecific medicines, we are exploring innovative approaches that have the potential to broaden patient reach and improve outcomes. This work represents an important step toward the next generation of radiopharmaceuticals," said Daniel Steiner, Ph.D., SVP of Targeted Radio Therapeutics at Molecular Partners.

Building on the success of its first “mono”-targeting Radio-DARPins, the Company is highlighting the ability to expand its impact in the field of RLT through multispecific DARPins. These can be formatted either as a bispecific (two DARPins each binding an individual target) or as a 2-in-1 DuoDARPin (one DARPin able to bind two tumor targets in an either/or manner).

The Company’s multispecific approaches enable the design of radiopharmaceuticals for effective treatment of highly heterogenous cancers, with target expression variability across tumor lesions and patients. Such bispecific radiopharmaceuticals could allow to treat cancer indications in which two targets are co-expressed solely on tumor tissues, creating tumor-specific solutions for patients with limited therapeutic options today.

Molecular Partners’ lead Radio-DARPin candidate MP0712, co-developed with Orano Med and targeting delta-like ligand 3 (DLL3), is in a multicenter US Phase 1/2a trial, building on the successful generation of first imaging and dosimetry data from a compassionate care program. The second candidate MP0726, targeting mesothelin MSLN, is differentiated by its ability to selectively bind membrane-bound MSLN, and work towards first human imaging is expected this year. Molecular Partners expects to announce a third Radio-DARPin program, targeting a different tumor target, in 2026.

Following today’s presentation, a copy of the presentation from the Gordon Research Conference will be available on Molecular Partners website, under Scientific Documents.

About Gordon Research Conferences
Founded in 1931, Gordon Research Conferences (GRC) is a nonprofit organization based in Rhode Island that organizes a series of internationally recognized scientific conferences across the biological, chemical, and physical sciences. GRC hosts hundreds of conferences annually, spanning fields from physics and neurobiology to materials science and medicine, and its meetings are known for fostering in-depth scientific discussion among leading researchers in each field. Attendance is limited and application-based, with participants selected by the conference chair, encouraging close interaction and community-building among scientists advancing the frontier of their fields.

About Radio-DARPins
Molecular Partners develops targeted alpha therapeutics leveraging its Radio-DARPins as isotope-agnostic vectors with the potential to unlock a broad range of cancer targets and indications. Molecular Partners designs its Radio-DARPin candidates matching disease and target biology with vector and isotope properties to address unmet medical needs. Building on the DARPins’ unique properties, Molecular Partners has developed a proprietary Radio-DARPin platform for precise delivery of potent radioactive payloads to tumor lesions. Molecular Partners’ Radio-DARPins address historic limitations of radioligand therapy, such as kidney accumulation and suboptimal tumor uptake, through optimized half-life extension and surface engineering approaches, while preserving the advantages of the small protein format. Molecular Partners has established partnerships with industry leaders covering the full value chain for the development of its Radio-DARPin therapeutics, including a strategic collaboration with Orano Med – pioneer in the development of 212Pb-based targeted alpha therapies (TAT), a non-exclusive development agreement with Eckert & Ziegler – global leader in radiopharmaceutical manufacturing, and a supply agreement with PanTera – a leading 225Ac radioisotope producer.

About Molecular Partners AG 
Molecular Partners AG (SIX: MOLN, NASDAQ: MOLN) is a clinical-stage biotech company pioneering a novel class of protein drugs known as DARPin therapeutics, for medical challenges other treatment modalities cannot readily address. Molecular Partners leverages the key properties of DARPins to design and develop differentiated therapeutics for cancer patients, including targeted radiopharmaceuticals and next-generation immune cell engagers. The Company has proprietary programs in various stages of pre-clinical and clinical development, as well as programs developed through partnerships with leading pharmaceutical companies and academic centers. Molecular Partners, founded in 2004, has offices in both Zurich, Switzerland and Concord, MA, USA. For more information, visit www.molecularpartners.com and find us on LinkedIn.

For further details, please contact:
Seth Lewis, EVP Corporate Finance
Concord, Massachusetts, U.S.
seth.lewis@molecularpartners.com
Tel: +1 781 420 2361

Laura Jeanbart, PhD, Head of Portfolio Management & Communications
Zurich-Schlieren, Switzerland
laura.jeanbart@molecularpartners.com
Tel: +41 44 575 19 35

Cautionary Note Regarding Forward-Looking Statements

This press release contains forward-looking statements. Any statements contained in this press release that do not describe historical facts may constitute forward-looking statements as that term is defined in the Private Securities Litigation Reform Act of 1995, as amended, including without limitation: implied and express statements regarding the clinical development of Molecular Partners’ current or future product candidates; expectations regarding timing for reporting data from ongoing clinical trials or the initiation of future clinical trials; the potential therapeutic and clinical benefits of Molecular Partners’ product candidates and its RDT and Switch-DARPin platforms; the selection and development of future programs; Molecular Partners’ collaboration with Orano Med including the benefits and results that may be achieved through the collaboration; the expected benefits of the strategic review; and Molecular Partners’ expected business and financial outlook, including anticipated expenses and cash utilization for 2026 and its expectation of its current cash runway. These statements may be identified by words such as “aim”, “anticipate”, “expect”, “guidance”, “intend”, “outlook”, “plan”, “potential”, “will” and similar expressions, and are based on Molecular Partners’ current beliefs and expectations. These statements involve risks and uncertainties that could cause actual results to differ materially from those reflected in such statements. Some of the key factors that could cause actual results to differ from Molecular Partners’ expectations include, but are not limited to, those set forth in under the heading “Risk Factors” in Molecular Partners’ Annual Report on Form 20-F for the year ended December 31, 2025 and other filings Molecular Partners makes with the SEC from time to time. These documents are available on the Investors page of Molecular Partners’ website at www.molecularpartners.com. In addition, this press release contains information relating to interim data as of the relevant data cutoff date, results of which may differ from topline results that may be obtained in the future.

Any forward-looking statements speak only as of the date of this press release and are based on information available to Molecular Partners as of the date of this release, and Molecular Partners assumes no obligation to, and does not intend to, update any forward-looking statements, whether as a result of new information, future events or otherwise.


FAQ

What did Molecular Partners (MOLN) present at the Gordon Research Conference on July 15, 2026?

Molecular Partners presented its bispecific and multispecific Radio-DARPin approaches for radioligand therapy on July 15, 2026. According to Molecular Partners, the presentation detailed how DARPins are engineered to match target and disease biology, addressing tumor heterogeneity and expanding radiopharmaceutical options for difficult-to-treat cancers.

How do Molecular Partners’ bispecific Radio-DARPins aim to improve cancer treatment for MOLN investors?

The bispecific Radio-DARPins are designed to engage multiple tumor targets simultaneously, potentially improving precision and therapeutic efficacy. According to Molecular Partners, formats include bispecific constructs and 2-in-1 DuoDARPins, intended to treat highly heterogeneous cancers with variable target expression across lesions and patients.

What is the status of Molecular Partners’ lead Radio-DARPin MP0712 (MOLN)?

MP0712, co-developed with Orano Med and targeting DLL3, is in a multicenter US Phase 1/2a trial. According to Molecular Partners, this follows successful imaging and dosimetry data from a compassionate care program, positioning MP0712 as the most advanced Radio-DARPin in its radioligand portfolio.

What distinguishes Molecular Partners’ Radio-DARPin candidate MP0726 for MSLN-positive tumors?

MP0726 targets mesothelin (MSLN) and is differentiated by selective binding to membrane-bound MSLN. According to Molecular Partners, work toward first human imaging is expected in 2026, supporting development as a radiopharmaceutical for cancers where mesothelin is expressed on tumor cell surfaces.

Is Molecular Partners (MOLN) planning additional Radio-DARPin programs after MP0712 and MP0726?

Yes, Molecular Partners expects to announce a third Radio-DARPin program targeting a different tumor antigen in 2026. According to Molecular Partners, this would expand its multispecific radiopharmaceutical pipeline beyond MP0712 and MP0726 in radioligand therapy for cancer.