Study of AMG 994 Monotherapy and AMG 994 and AMG 404 Combination Therapy in Participants With Advanced Solid Tumors

  • STATUS
    Not Recruiting
  • End date
    Aug 6, 2025
  • participants needed
    214
  • sponsor
    Amgen
Updated on 23 May 2022

Summary

The primary objective of this study is to evaluate the safety, tolerability, and maximum tolerated dose (MTD)/maximum tolerated combination dose (MTCD) or recommended phase 2 dose (RP2D) of AMG 994 as monotherapy and AMG 994 in combination with AMG 404 in participants with advanced solid tumors.

Description

AMG 994 will be administered by short term intravenous (IV) infusion once weekly in each 28-day cycle and AMG 404 will be administered by short-term IV infusion once every 4 weeks (Q4W) in a 28 day cycle (on day 1 of cycle 2 and beyond). The study will be conducted in 2 parts: Part 1 - Dose Exploration and Part 2 - Dose Expansion.

Details
Condition Advanced Solid Tumors
Treatment AMG 404, AMG 994
Clinical Study IdentifierNCT04727554
SponsorAmgen
Last Modified on23 May 2022

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