Molecular Partners
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Molecular Partners (MOLN) investor relations material

Molecular Partners Q4 2025 earnings summary

Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.
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Q4 2025 earnings summary12 Mar, 2026

Executive summary

  • Advanced clinical pipeline in oncology, focusing on DARPin-based targeted radiotherapies and immune cell engagers, including MP0712 for SCLC/NECs and MP0726 for ovarian cancer, both in collaboration with Orano Med.

  • Initiated US Phase 1/2a study of DLL3-targeting Radio-DARPin MP0712 for SCLC and neuroendocrine cancers; initial data expected in 2026.

  • Advanced MP0726 targeting MSLN towards first-in-human imaging; new candidate nominations anticipated mid-2026.

  • Signed development agreement with Eckert & Ziegler to expand Radio-DARPin pipeline with a range of isotopes, including 225Ac.

  • Strategic review completed, extending cash runway into 2028 and resulting in organizational changes and cost reductions.

Financial highlights

  • Cash balance of CHF 93.1 million as of December 31, 2025, down from CHF 149.4 million in 2024, supporting operations through 2028.

  • Net cash used in operations was CHF 51.3 million in 2025, an improvement from CHF 59.2 million in 2024.

  • Operating loss of CHF 58.1 million in 2025, including CHF 2.6 million restructuring charge.

  • Revenues of CHF 5.0 million in 2025, compared to zero in 2024.

  • Shareholders' equity CHF 80.3 million (2024: CHF 141.6 million); company remains debt-free.

Outlook and guidance

  • MP0712 Phase 1/2a study open in the US, with initial safety data expected in H1 2026 and activity data in H2 2026.

  • Progression of MP0726 to first-in-human imaging and nomination of new RDT programs planned for mid-2026.

  • Updates on MP0533 and Switch-DARPin programs anticipated in H1 2026.

  • Operating expenses for 2026 expected at CHF 45–55 million, including CHF 6 million in non-cash costs.

Rationale for evaluating 225 Ac isotopes
MP0533 selectivity mechanism for AML cells
Role of FAP anchoring in MP0317 localization
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