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Clinical Trials in the EU / 2025-521702-18-00
Authorised, recruiting Phase I

A phase I open-label, multi-center study to evaluate the safety, tolerability, dosimetry, and preliminary activity of [177Lu]Lu-DFC413 and safety and imaging properties of [68Ga]Ga-NNS309 in patients with solid tumors

2025-521702-18-00 · tracked via the Priya Life Science EU tracker
Sponsor
Novartis Pharma AG
Sponsor type
Pharmaceutical company
Therapeutic area
Neoplasms
Decision date
16/02/2026
Enrollment target
62
Sites
Germany, Portugal, France, Spain, Denmark

Condition studied

Locally advanced unresectable or metastatic soft tissue sarcoma (excluding GIST and Kaposi sarcoma), Locally advanced unresectable or metastatic pancreatic ductal adenocarcinoma (PDAC), Locally advanced unresectable or metastatic non-small cell lung cancer (NSCLC), Locally advanced unresectable or metastatic colorectal cancer (CRC), Locally advanced unresectable or metastatic triple negative breast cancer (TNBC), Locally advanced unresectable or metastatic HR+/HER2- ductal or lobular breast cancer (BC)

Eligibility

Age group
18-64 years, 65+ years
Sex
Female, Male
Official registry record

This page summarises publicly available CTIS data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View 2025-521702-18-00 on CTIS ↗ ← All trials in the EU