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A Study of TAS2940 in Participants With Locally Advanced or Metastatic Solid Tumor Cancer

Phase 1
Active, not recruiting
Conditions
Breast Cancer
Solid Tumor
Glioblastoma
Non-small Cell Lung Cancer
Interventions
Registration Number
NCT04982926
Lead Sponsor
Taiho Oncology, Inc.
Brief Summary

This is a first-in-human, open label, multicenter study to assess the safety, tolerability, pharmacokinetics, pharmacodynamics, and the preliminary antitumor activity of TAS2940 in patients with advanced or metastatic solid tumors who are not candidates for approved or available therapies.

Detailed Description

TAS2940 is a small molecule inhibitor of ERBB family proteins HER2 and EGFR. It has not been evaluated in human subjects yet. The study will be conducted in 2 parts, dose escalation and dose expansion. The dose escalation part will assess the safety and determine the maximum tolerated dose, the recommended phase 2 dose and the recommended dosing regimen of TAS2940 administered orally. The dose expansion part will assess preliminary anti-tumor activity in select solid tumors characterized by HER2 or EGFR aberrations.

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
42
Inclusion Criteria
  • Have histologically confirmed solid cancer that is locally advanced and metastatic and available standard treatment options have been exhausted
  • Have adequate organ function
  • ECOG PS 0-1

Dose Escalation:

  • Have measurable or non- measurable disease per RECIST criteria v1.1 or RANO
  • Any solid tumor with EGFR and / or HER2 aberration

Dose Expansion:

  • Have measurable disease per RECIST criteria v1.1 for solid tumor (excluding primary brain tumor) or RANO (for glioblastoma)
  • Cohort A: Non-small cell lung cancer (NSCLC)
  • Cohort B: HER2 positive breast cancer
  • Cohort C: Recurrent or refractory glioblastoma
  • Cohort D: Other solid tumors with EGFR or HER2 aberrations
Exclusion Criteria
  • Non-stable brain metastases
  • Have significant cardiovascular disorder
  • Have not recovered from prior cancer treatment
  • A serious illness or medical condition

Study & Design

Study Type
INTERVENTIONAL
Study Design
SEQUENTIAL
Arm && Interventions
GroupInterventionDescription
Dose Expansion GliblastomaTAS2940Dose expansion will assess preliminary anti-tumor activity in select solid tumors characterized by HER2 or EGFR aberrations.
Dose Expansion Solid tumorsTAS2940Dose expansion will assess preliminary anti-tumor activity in select solid tumors characterized by HER2 or EGFR aberrations.
Dose Expansion Non-small Cell Lung CancerTAS2940Dose expansion will assess preliminary anti-tumor activity in select solid tumors characterized by HER2 or EGFR aberrations
TAS2940 Dose EscalationTAS2940Dose escalation will assess the safety and determine the maximum tolerated dose, the recommended phase 2 dose and the recommended dosing regimen of TAS2940 administered orally.
Dose Expansion Breast CancerTAS2940Dose expansion will assess preliminary anti-tumor activity in select solid tumors characterized by HER2 or EGFR aberrations
Primary Outcome Measures
NameTimeMethod
Dose Escalation:Maximum Tolerated Dose (MTD)One Month

Determine the incidence of dose-liming toxicities (DLTs) and adverse events (AEs) graded according to National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) v5.0 within the first cycle

Dose Expansion:Overall Response Rate6 Months

Document the ORR, defined as proportion of patients experiencing a best overall response of Complete Response (CR) or Partial response (PR) based on investigator accessed radiographic response per RECIST 1.1 or RANO criteria

Secondary Outcome Measures
NameTimeMethod
Dose Expansion:Pharmacokinetic profile of TAS29403 Months

Evaluation of the maximum observed plasma concentration; time to reach maximum concentration, area under the Concentration-time curve and time it takes for plasma concentration to fall by half its original value (T1/2) of TAS2940

Dose Expansion:Progression Free Survival (PFS)Estimated up to 6 months

Date of PR or CR to date of objective progression or death due to any cause.

Dose Escalation: Overall Response Rate (ORR)6 Months

Document the ORR defined as proportion of patients experiencing a best overall response of Complete Response (CR) or Partial response (PR) based on investigator accessed radiographic response per RECIST 1.1 or RANO criteria

Dose Expansion:Incidence of treatment-emergent Adverse Events (Safety and tolerability)Estimated up to 6 months

Safety and tolerability of TAS2940 based on reported AEs, graded according to NCI-CTCAE v.5.0

Dose Expansion:Duration of Response (DOR)Estimated up to 6 months

DOR, defined as time from the first documentation of response to date of objective tumor progression or death due to any cause, whichever occurs first.

Dose Expansion:Disease Control Rate (DCR)Estimated up to 6 months

DCR, defined as the proportion of patients experiencing a best overall response of Stable Disease (SD), PR or CR

Dose Escalation:Pharmacokinetic (PK) Profile3 Months

Evaluation of the maximum observed plasma concentration; time to reach maximum concentration, area under the Concentration-time curve and time it takes for plasma concentration to fall by half its original value (T1/2) of TAS2940

Trial Locations

Locations (3)

Tennessee Oncology

🇺🇸

Nashville, Tennessee, United States

University of Texas MD Anderson Cancer Center

🇺🇸

Houston, Texas, United States

CLCC Gustave Roussy

🇫🇷

Villejuif, Cedex, France

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