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Jul 6, 2026Clinical readout

Molecular Partners updates on DLL3 and MSLN Radio-DARPin programs

The company reported ongoing dosing in the MP0712 Phase 1/2a trial and a new South African compassionate-care program using a different isotope pairing for DLL3 targeting.

Molecular Partners AG said on July 6, 2026 that dosing of patients is ongoing in the first cohort of the US multicenter Phase 1/2a study of MP0712, which targets DLL3 and carries the payload Lead-212, developed with Orano Med for small cell lung cancer and other neuroendocrine cancers1. The Phase 1 study contains up to 4 dose levels, with each patient receiving up to 4 doses within their assigned dose level, and five centers are currently open and recruiting1. Initial data from the study are expected within the next months, with a more comprehensive dataset on safety and efficacy expected in 20271.

Separately, the company disclosed a new compassionate-care initiative in South Africa. Dr. Mike Sathekge of the Nuclear Medicine Research Institute in South Africa requested an early-access clinical program, under Section 21 of the country's Medicines and Related Substances Act, using a DLL3-targeting Radio-DARPin referred to as MP0714. In this program, 177Lu is used to image patients while 225Ac is used to treat them, functioning as a theranostic pair1. Molecular Partners said it remains fully focused on executing the US Phase 1/2a study of MP0712 with 212Pb1, distinguishing that trial from the South African compassionate-care effort. PanTera, a radioisotope producer, is among the suppliers of 225Ac for MP0714's use at the Nuclear Medicine Research Institute1.

On the company's second radiopharmaceutical candidate, MP0726 targets mesothelin, a tumor target overexpressed in several cancers including ovarian cancer, and the company plans to advance it toward first-in-human imaging in the second half of 20261. The company also plans two INDs across its pipeline in 2027 and expects to nominate a new radiotherapeutic target in the second half of this year1.

Written by readthrough’s AI from the linked primary sources and fact-checked against them automatically before publishing. Not investment advice.