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NCT Number: NCT06360354

A Study Evaluating Anvumetostat in Combination With Other Therapies in Participants With Advanced Gastrointestinal, Biliary Tract, or Pancreatic Cancers With Homozygous Methylthioadenosine Phosphorylase (MTAP)-Deletion (MTAPESTRY 103)

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.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

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Key information

Age range

18 year–100 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Chris OBrien Lifehouse, Camperdown, New South Wales, Australia

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Subprotocol B

Inclusion:

  • Age ≥ 18 years (or ≥ legal age within the country if it is older than 18 years).
  • Histologically or cytologically confirmed diagnosis of metastatic and/or unresectable (locally advanced) adenocarcinoma of the pancreas.
  • Tumor tissue (FFPE sample) or an archival block must be available. Participants without archived tumor tissue available may be allowed to enroll by undergoing tumor biopsy before dosing.
  • Homozygous MTAP-deletion.
  • Disease measurable as defined by RECIST v1.1.
  • Adequate organ function as defined in the protocol.

Exclusion:

  • Prior treatment with a MAT2A inhibitor or a PRMT5 inhibitor.
  • Radiation therapy within 28 days of first dose.
  • Major surgery within 28 days of first dose of Anvumetostat.
  • Cardiovascular and pulmonary exclusion criteria as defined in the protocol.
  • Gastrointestinal tract disease causing the inability to take PO medication, malabsorption syndrome, requirement for IV alimentation, gastric/jejunal tube feeds, uncontrolled inflammatory gastrointestinal disease (eg, Crohn's disease, ulcerative colitis).
  • History of solid organ transplantation.

Subprotocol C

Inclusion:

  • Age ≥ 18 years (or ≥ legal age within the country if it is older than 18 years).
  • Histologically or cytologically confirmed diagnosis of metastatic and/or unresectable (locally advanced) adenocarcinoma of the pancreas.
  • Homozygous MTAP-deletion.
  • Rat Sarcoma Viral Oncogene Homolog (RAS) mutation
  • Received at least 1 prior systemic therapy for advanced or metastatic PDAC.
  • Disease measurable as defined by RECIST v1.1.
  • Adequate organ function as defined in the protocol.

Exclusion:

  • Prior treatment with aMAT2A inhibitor, a PRMT5 inhibitor, or a MAPK pathway inhibitor, including KRAS inhibitors.
  • Cardiovascular and pulmonary exclusion criteria as defined in the protocol.
  • Gastrointestinal tract disease causing the inability to take PO medication, malabsorption syndrome, requirement for IV alimentation, gastric/jejunal tube feeds, uncontrolled inflammatory gastrointestinal disease (eg, Crohn's disease, ulcerative colitis).
  • History of solid organ transplantation.

Treatment and study plan

Anvumetostat

Drug

Administered Orally

Other names: AMG 193

Gemcitabine

Drug

Administered IV

Nab-paclitaxel

Drug

Administered IV

Modified FOLFIRINOX

Drug

Modified FOLFIRINOX consists of irinotecan, 5-FU, LV, and oxaliplatin administered IV

RMC-6236

Drug

Administered orally

Primary outcomes

  1. Number of Participants Experiencing Dose Limiting Toxicities (DLT)

    Time frame: Up to 28 days

  2. Number of Participants Experiencing Treatment Emergent Adverse Events (TEAE)

    Time frame: Up to approximately 2 years

    Any clinically significant changes in vital signs, electrocardiogram, or lab parameters will be recorded as TEAEs.

  3. Number of Participants Experiencing Serious Adverse Events (SAE)

    Time frame: Up to approximately 2 years

Secondary outcomes

  1. Objective Response (OR) per Response Evaluation Criteria in Solid Tumors (RECIST v1.1)

    Time frame: Up to approximately 2 years

  2. Disease Control (DC) per RECIST v1.1

    Time frame: Up to approximately 2 years

  3. Duration of Response (DOR) per RECIST v1.1

    Time frame: Up to approximately 2 years

  4. Time to Response (TTR) per RECIST v1.1

    Time frame: Up to approximately 2 years

  5. Overall Survival (OS) per RECIST v1.1

    Time frame: Up to approximately 2 years

  6. Progression-free Survival (PFS) per RECIST v1.1

    Time frame: Up to approximately 2 years

  7. Maximum Plasma Concentration (Cmax) of Anvumetostat

    Time frame: Up to Day 1 of Cycle 5 (one cycle = 21 or 28 days)

  8. Time to Maximum Plasma Concentration (tmax) of Anvumetostat

    Time frame: Up to Day 1 of Cycle 5 (one cycle = 21 or 28 days)

  9. Area Under the Plasma Concentration-time Curve (AUC) of Anvumetostat

    Time frame: Up to Day 1 of Cycle 5 (one cycle = 21 or 28 days)

  10. Cmax of RMC-6236

    Time frame: Up to Day 1 of Cycle 5 (one cycle = 21 days)

  11. Tmax of RMC-6236

    Time frame: Up to Day 1 of Cycle 5 (one cycle = 21 days)

  12. AUC of RMC-6236

    Time frame: Up to Day 1 of Cycle 5 (one cycle = 21 days)

Sponsors and collaborators

Lead sponsor

Amgen

Industry

Registry information

Official study title

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

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Apr 11, 2024
Registry last updated
Jun 1, 2026

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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