A Phase 1 Study Evaluating the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Efficacy of AMG 211 Administered as Continuous Intravenous Infusion in Subjects With Relapsed/Refractory Gastrointestinal Adenocarcinoma
Latest Information Update: 18 Mar 2021
At a glance
- Drugs MEDI 565 (Primary)
- Indications Adenocarcinoma; Cholangiocarcinoma; Gastrointestinal cancer; Pancreatic cancer
- Focus Adverse reactions
- Sponsors Amgen
- 23 Feb 2021 Status changed to discontinued.
- 03 Feb 2021 Number of arms changed from 1 to 11. Study design changed from Single Group Assignment to Sequential Assignment. Allocation changed to Non-Randomized.
- 11 Jan 2018 Status changed from active, no longer recruiting to completed.