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OpenTrials
Active, Not Recruiting

NCT Number: NCT05669482

Study of Avutometinib (VS-6766) +Defactinib With Gemcitabine and Nab-paclitaxel in Patients With Pancreatic Cancer

This study will assess the safety and efficacy of avutometinib (VS-6766) and defactinib in combination with gemcitabine and nab-paclitaxel in patients with Pancreatic Ductal Adenocarcinoma (PDAC) who have been previously untreated.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

UCSF Helen Diller Family Comprehensive Cancer Center, San Francisco, California, United States

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About this study

This is a multicenter, non-randomized, open-label Phase 1/2 study designed to evaluate safety, tolerability and efficacy of avutometinib (VS-6766) and defactinib in combination with gemcitabine and nab-paclitaxel in patients previously untreated metastatic Pancreatic Ductal Adenocarcinoma (PDAC).

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Male or female subjects ≥ 18 years of age
  • Histologic or cytologic evidence of metastatic pancreatic ductal adenocarcinoma.
  • An Eastern Cooperative Group (ECOG) performance status ≤ 1
  • Measurable disease according to RECIST 1.1
  • Adequate organ function
  • Adequate cardiac function
  • Agreement to use highly effective method of contraceptive

Exclusion criteria

  • Patients with pancreatic neuroendocrine tumors
  • Prior or concomitant treatment for metastatic pancreatic ductal adenocarcinoma
  • Prior treatment with inhibitors of the RAS /MAPK pathway [e.g. MEK inhibitors] or inhibitors of FAK
  • History of prior malignancy, with the exception of curatively treated malignancies
  • Major surgery within 4 weeks (excluding placement of vascular access)
  • Concurrent heart disease or severe obstructive pulmonary disease
  • Concurrent ocular disorders
  • Active skin disorder that has required systemic therapy within the past 1 year
  • Patients with interstitial lung disease or pulmonary fibrosis or severe lung disease, pulmonary edema, and adult respiratory distress syndrome
  • Known SARS-Cov2 infection ≤28 days prior to first dose of study therapy

Treatment and study plan

avutometinib (VS-6766) and defactinib in combination with gemcitabine and nab-paclitaxel

Drug

The RP2D of avutometinib (VS-6766) and defactinib in combination with gemcitabine and nab-paclitaxel determined in Part A will be used in Part B dose expansion.

Other names: Gemzar, Abraxane

Primary outcomes

  1. Part A: To determine RP2D for avutometinib (VS-6766) and defactinib in combination gemcitabine and nab-paclitaxel

    Time frame: 28 days

    Assessment of Dose-limiting toxicities (DLTs)

  2. To determine the efficacy of the RP2D identified in Part A

    Time frame: 6 months

    Confirmed overall response rate (ORR) (partial response [PR] + complete response [CR] defined according to Response Evaluation Criteria in Solid Tumors version 1.1 [RECIST 1.1])

Secondary outcomes

  1. Duration of Response (DOR)

    Time frame: 24 months

    Time of first response to PD as assessed per RECIST 1.1

  2. Disease Control Rate (DCR)

    Time frame: 24 months

    CR + PR + SD as assessed per RECIST 1.1

  3. Progression Free Survival (PFS)

    Time frame: 24 months

    From the time of first dose of study intervention to PD as assessed per RECIST 1.1 or death from any cause

  4. Overall Survival (OS)

    Time frame: Up to 5 years

    From the time of first dose of study intervention to PD as assessed per RECIST 1.1 or death from any cause

  5. Plasma Pharmacokinetics (PK) of avutometinib (VS-6766) and Defactinib and relevant metabolites, Tmax

    Time frame: 10 weeks

    Time to Maximum concentration (Tmax)

  6. Plasma Pharmacokinetics (PK) of avutometinib (VS-6766) and Defactinib and relevant metabolites, AUC

    Time frame: 10 Weeks

    Area under plasma Concentration (AUC) 0 to t

  7. Plasma Pharmacokinetics (PK) of avutometinib (VS-6766) and Defactinib and relevant metabolites, Half-life

    Time frame: 10 weeks

    concentration Half-life (T1/2)

  8. Frequency and severity adverse events (AEs) and Serious Adverse Events (SAEs)

    Time frame: 24 months

    Count of AE and SAEs by grade, based on the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) grading scale

  9. Number of abnormal laboratory values

    Time frame: 24 months

    Count of abnormal laboratory values by grade

Sponsors and collaborators

Lead sponsor

Verastem, Inc.

Industry

Registry information

Official study title

A Phase 1b/2a Study of Gemcitabine and Nab-paclitaxel in Combination With Avutometinib (VS-6766) and Defactinib in Patients With Previously Untreated Metastatic Adenocarcinoma of the Pancreas

Acronym: RAMP205

Important dates

Study start
2023
Primary completion
2026
Study completion
2027
First posted
Dec 30, 2022
Registry last updated
Sep 2, 2025

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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