Anvumetostat
DrugAdministered Orally
Other names: AMG 193
NCT Number: NCT06360354
The study aims to determine maximum tolerated dose (MTD) or recommended combination dose of the MTA-cooperative PRMT5 inhibitor Anvumetostat administered in combination with other therapies in adult participants with metastatic or locally advanced methylthioadenosine phosphorylase (MTAP)-deleted gastrointestinal, biliary tract, or pancreatic cancers. The study also aims to determine the safety profile of Anvumetostat administered in combination with other therapies in adult participants with metastatic or locally advanced MTAP-deleted gastrointestinal, biliary tract, or pancreatic cancers.
This study is active but is not currently recruiting participants.
Notify Me18 year–100 year
All sexes
Interventional
Phase 1
Chris OBrien Lifehouse, Camperdown, New South Wales, Australia
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Subprotocol B
Inclusion:
Exclusion:
Subprotocol C
Inclusion:
Exclusion:
Administered Orally
Other names: AMG 193
Administered IV
Administered IV
Modified FOLFIRINOX consists of irinotecan, 5-FU, LV, and oxaliplatin administered IV
Administered orally
Time frame: Up to 28 days
Time frame: Up to approximately 2 years
Any clinically significant changes in vital signs, electrocardiogram, or lab parameters will be recorded as TEAEs.
Time frame: Up to approximately 2 years
Time frame: Up to approximately 2 years
Time frame: Up to approximately 2 years
Time frame: Up to approximately 2 years
Time frame: Up to approximately 2 years
Time frame: Up to approximately 2 years
Time frame: Up to approximately 2 years
Time frame: Up to Day 1 of Cycle 5 (one cycle = 21 or 28 days)
Time frame: Up to Day 1 of Cycle 5 (one cycle = 21 or 28 days)
Time frame: Up to Day 1 of Cycle 5 (one cycle = 21 or 28 days)
Time frame: Up to Day 1 of Cycle 5 (one cycle = 21 days)
Time frame: Up to Day 1 of Cycle 5 (one cycle = 21 days)
Time frame: Up to Day 1 of Cycle 5 (one cycle = 21 days)
Amgen
Industry
A Phase 1b Study Evaluating the Safety, Tolerability, Pharmacokinetics, and Efficacy of Anvumetostat in Combination With Other Therapies in Subjects With Advanced Gastrointestinal, Biliary Tract, or Pancreatic Cancers With Homozygous MTAP-deletion
Acronym: MTAPESTRY 103
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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