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Phase 1 First-In-Human Study to Explore the Safety, Tolerability, and Pharmacokinetics of AMG 305 in Subjects With Advanced Solid Tumors

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2022-502867-39-00
Acronym
20220073
Enrollment
58
Registered
2023-08-23
Start date
2023-09-29
Completion date
2025-12-12
Last updated
2025-06-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Advanced solid tumors including non-small cell lung cancer (NSCLC), cervical carcinoma, head and neck carcinoma, mesothelioma, ovarian cancer, pancreatic adenocarcinoma, uterine carcinoma and breast cancer.

Interventions

None listed

Sponsors

Amgen Inc.
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Countries

France, Germany, Spain

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026