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Clinical Trials/NCT04521413
NCT04521413
Active, not recruiting
Phase 1

A First-In-Human, Phase 1/2 Study Of CFI-402411, a Hematopoietic Progenitor Kinase-1 (HPK1) Inhibitor, as a Single Agent and in Combination With Pembrolizumab in Subjects With Advanced Solid Malignancies

Treadwell Therapeutics, Inc13 sites in 3 countries170 target enrollmentStarted: August 31, 2020Last updated:

Overview

Phase
Phase 1
Status
Active, not recruiting
Enrollment
170
Locations
13
Primary Endpoint
To examine best overall response rate in subjects treated at multiple dose levels of CFI-402411.

Overview

Brief Summary

The purpose of this study is to test the safety of an investigational drug called CFI-402411 alone and in combination with pembrolizumab and to study its effects in patients with advanced solid tumors who have progressed following previous therapies.

Detailed Description

This study will be a first-in-human study evaluating the safety and tolerability of CFI-402411 in subjects with advanced solid malignancies, when CFI-402411 is administered as a single agent or in combination with pembrolizumab. CFI-402411 is an oral pill that blocks the function of HPK1. Blocking HPK1 could stimulate an immune response against the tumor in patients. This immune response could be further enhanced when combined with pembrolizumab. The data obtained from this study will determine the dose and schedule and subject selection for further clinical studies.

Pre-clinical findings support further development of CFI-402411 as a novel anti-cancer agent, and the combination of CFI-402411 with pembrolizumab as a potential strategy to improve outcomes of subjects with advanced malignancies.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Sequential
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Study-Wide Eligibility (Across All Study Parts):
  • Age \> 18 years old
  • Have progressed after ≥ 1, but no more than 3 regimens of systemic therapies for recurrent / metastatic disease.
  • Subjects must have measurable disease.
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
  • Part A1: Monotherapy Dose Escalation Inclusion Criteria
  • Histological or cytological confirmation of advanced solid malignancy that is refractory to or not a candidate for current standard treatment(s) and for whom no standard therapy is available.
  • Part A2: Biomarker-Focused Monotherapy Backfills Inclusion Criteria
  • Histological or cytological confirmation of one of the advanced cancers listed below;
  • cutaneous melanoma

Exclusion Criteria

  • Study-Wide Eligibility (Across All Study Parts)
  • Subjects will be excluded from the study if any of the following criteria is met;
  • Previous treatment with an HPK1 inhibitor in other clinical trials.
  • Diagnosis of autoimmune-based disease or clinically significant auto-immune disorders.
  • Have symptomatic congestive heart failure, active angina pectoris or recent myocardial infarction (within 6 mos).
  • Have chronic atrial fibrillation.
  • Known central nervous system metastasis.
  • Stroke or transient ischemic attack, or other ischemic events or thromboembolic events within 3 months of study enrollment.
  • A history of QTc prolongation or a marked baseline prolongation of QT/QTc interval or a history of additional risk factors for TdP (e.g., heart failure, hypokalemia, family history of Long QT Syndrome).

Arms & Interventions

A1: Monotherapy Escalation

Experimental

Dose escalation arm with CFI-402411. CFI-402411 is administered orally once daily.

Intervention: CFI-402411 (Drug)

A2: Monotherapy Biomarker

Experimental

Dose escalation biomarker arm with CFI-402411. CFI-402411 is administered orally once daily.

Intervention: CFI-402411 (Drug)

A3: Monotherapy Expansion

Experimental

Dose expansion arm with CFI-402411 at its recommended phase 2 dose.

Intervention: CFI-402411 (Drug)

B1: Combination Escalation

Experimental

Dose escalation arm with CFI-402411 in combination with pembrolizumab (at its labeled dose and schedule).

Intervention: CFI-402411 (Drug)

B1: Combination Escalation

Experimental

Dose escalation arm with CFI-402411 in combination with pembrolizumab (at its labeled dose and schedule).

Intervention: Pembrolizumab (Drug)

B2: Combination Expansion

Experimental

Dose expansion arm with the recommended phase 2 dose of CFI-402411 in combination with pembrolizumab (at its labeled dose and schedule).

Intervention: CFI-402411 (Drug)

B2: Combination Expansion

Experimental

Dose expansion arm with the recommended phase 2 dose of CFI-402411 in combination with pembrolizumab (at its labeled dose and schedule).

Intervention: Pembrolizumab (Drug)

Outcomes

Primary Outcomes

To examine best overall response rate in subjects treated at multiple dose levels of CFI-402411.

Time Frame: 48 months

Best overall response rate will be summarized by dose cohort and overall using the percent of patients in each tumor response category.

To examine progression free survival in subjects treated at multiple dose levels of CFI-402411.

Time Frame: 48 months

Time from first dose to disease progression or death whichever occurs first will be calculated and summarized for all patients by dose cohort and overall.

To assess the incidence of adverse events of CFI-402411 as a single agent and at the recommended phase 2 dose (RP2D).

Time Frame: 48 months

The number of subjects who experience an adverse event that was possibly related to study drug.

To assess the incidence of adverse events with CFI-402411 in combination with pembrolizumab and at the RP2D.

Time Frame: 48 months

The number of subjects who experience an adverse event that was possibly related to study drug.

Secondary Outcomes

  • To further assess the incidence of adverse events of CFI-402411.(48 months)
  • To assess duration of response of CFI-402411 monotherapy and in combination with pembrolizumab.(48 months)
  • To evaluate the effect of CFI-402411 treatment on immune- or disease related biomarkers.(48 months)
  • To identify the maximum tolerated dose of single agent CFI-402411 alone and in combination with pembrolizumab.(48 months)
  • To assess the pharmacokinetic profile of CFI-402411 alone when it is administered in combination with pembrolizumab through AUC.(48 months)
  • To assess the pharmacokinetic profile of CFI-402411 alone when it is administered in combination with pembrolizumab through Cmax.(48 months)
  • To assess best overall response of CFI-402411 monotherapy and in combination with pembrolizumab.(48 months)
  • To assess overall survival of CFI-402411 monotherapy and in combination with pembrolizumab.(48 months)
  • To assess the pharmacokinetic profile of CFI-402411 alone when it is administered in combination with pembrolizumab through Tmax.(48 months)
  • To assess the pharmacokinetic profile of CFI-402411 alone when it is administered in combination with pembrolizumab though Cmin.(48 months)
  • To assess the pharmacokinetic profile of CFI-402411 alone when it is administered in combination with pembrolizumab through T1/2.(48 months)
  • To assess overall response rates of CFI-402411 monotherapy and in combination with pembrolizumab.(48 months)
  • To assess progression free survival of CFI-402411 monotherapy and in combination with pembrolizumab.(48 months)

Investigators

Sponsor Class
Industry
Responsible Party
Sponsor

Study Sites (13)

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