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Anvumetostat Alone or in Combination With Other Therapies in Subjects With Advanced Thoracic Tumors With Homozygous MTAP-deletion (Master Protocol) (MTAPESTRY 104).

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NCT06333951 · readout in 72 d

Sponsored by Amgen (industry) · AMGN — their whole pipeline →.

Phase
Phase 1
Status
Active, not recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
49actual
Sites
83
Countries
Argentina, Australia, Austria +17

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2024-09-17actualWhen the study began enrolling
Primary completion2026-10-31estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2026-11-30estimatedThe whole study's end, after follow-up
First posted2024-03-27actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-05-28actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Thoracic Tumors
  • Non-small Cell Lung Cancer

Interventions

  • Drug: Anvumetostat — also filed as AMG 193
  • Drug: Carboplatin
  • Drug: Paclitaxel
  • Drug: Pembrolizumab
  • Drug: Pemetrexed
  • Drug: Sotorasib

Primary outcomes

what the primary-completion date above is the date OF
Number of Participants Experiencing Dose Limiting Toxicities (DLT)
measured Up to approximately 21 days
Number of Participants Experiencing Treatment Emergent Adverse Events (TEAE)
measured Up to approximately 3 years
Number of Participants Experiencing Serious Adverse Events (SAE)
measured Up to approximately 3 years

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