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FAK Inhibitor

AMP945 for Pancreatic Cancer

Phase 1 & 2
Recruiting
Research Sponsored by Amplia Therapeutics Limited
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up from first dose of study drug to end of study, an expected average of 6 months
Awards & highlights

Summary

This is a multicentre, open label, two-part study to determine whether the focal adhesion kinase (FAK) inhibitor AMP945, when given prior to dosing with gemcitabine and nab-paclitaxel, improves response to therapy in first-line patients with unresectable or metastatic pancreatic cancer. Part A is a phase 1b dose-escalation design that will enrol at least 3 participants in each of 4 dose-level cohorts, to determine the RP2D of AMP945 to be explored in Part B. Part B will determine the efficacy of the AMP945 regimen at the RP2D, and will be run as a Simon Two-stage design; Stage 1 will enrol 26 participants. If ≤5 of the 26 participants show an objective response, then recruitment will be paused and a detailed analysis of futility will be performed. If the study is deemed futile, recruitment will cease. If the study is determined to be not futile or \>5 of the 26 participants show an objective response, recruitment will continue, and an additional 24 participants will be enrolled in Stage 2.

Eligible Conditions
  • Pancreatic Cancer

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~from first dose of study drug to end of study, an expected average of 6 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and from first dose of study drug to end of study, an expected average of 6 months for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Number of Participants with Treatment-Emergent Adverse Events (TEAEs) from Baseline to End of Study
Part A: Determination of RP2D
Part B: efficacy of AMP945
Secondary study objectives
AMP945 levels in plasma
Part A: efficacy of AMP945
Other study objectives
Clinical benefit rate (CBR)
Duration of response (DOR)
Effects on biomarkers
+5 more

Trial Design

1Treatment groups
Experimental Treatment
Group I: AMP945Experimental Treatment2 Interventions
Part A: AMP945 administered in dose escalating cohorts Part B: AMP945 recommended phase 2 dose

Find a Location

Who is running the clinical trial?

Amplia Therapeutics LimitedLead Sponsor
~12 spots leftby May 2025