TerminatedPhase 1NCT04849273

A Study of TPX-0131, a Novel Oral ALK Tyrosine Kinase Inhibitor, in Patients With ALK+ Advanced or Metastatic NSCLC

A phase 1, first-in-human, open-label study to evaluate the safety, tolerability, PK, and efficacy of the novel ALK inhibitor TPX-0131 in pretreated subjects with ALK+ advanced or metastatic non-small cell lung cancer (NSCLC).

Checked against the public recordLast updated May 26, 2023 · Source: ClinicalTrials.gov

StatusTerminated
PhasePhase 1
U.S. locations15
SponsorTurning Point Therapeutics, Inc.
01
Study overview

What this study is about

Purpose
Treatment
Study type
Interventional
Phase
Phase 1
Sponsor
Turning Point Therapeutics, Inc.
Interventions being studied
Drug: TPX-0131
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

03
Public criteria

Who may be able to participate

Inclusion Criteria: * Age ≥ 18 (or as required by local regulation). * Histological or cytological confirmation of advanced/metastatic ALK+ NSCLC. * Pretreated with up to three prior lines of an ALK TKI treatment, including at least one prior line of a second or third-generation ALK TKI (alectinib, brigatinib, ensartinib, or lorlatinib) in Phase 1. * ECOG performance status ≤ 1. * Existence of measurable or evaluable disease (according to Response evaluation criteria in solid tumors \[RECIST v1.1\] criteria). * Subjects with asymptomatic CNS metastases and/or asymptomatic leptomeningeal carcinomatosis are eligible. * Adequate organ function. Exclusion Criteria: * Major surgery within four weeks of the start of TPX-0131 treatment. * Clinically significant cardiovascular disease * Any of the following cardiac criteria: * Mean resting corrected QT interval (QTc) \> 470 msec obtained from three ECGs and any factors that increase the risk of QTc prolongation or arrhythmic events * Any clinically important abnormalities in rhythm, conduction, or morphology of resting ECG * Known clinically significant active infections not controlled with systemic treatment (bacterial, fungal, viral including HIV positivity). * Gastrointestinal disease or other malabsorption syndromes that would impact drug absorption. * Subjects being treated with or anticipating the need for treatment with strong CYP3A4 inhibitors or inducers. * Subjects with current or anticipated need for drugs that are sensitive CYP2C9 substrates with narrow therapeutic indices.

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • Local Institution - 2104Orange, California
  • Local Institution - 2105Aurora, Colorado
  • Local Institution - 2106Boston, Massachusetts
  • Local Institution - 2108Boston, Massachusetts
  • Local Institution - 2103Hackensack, New Jersey
  • Local Institution - 2107Nashville, Tennessee
  • Local Institution - 2102Fairfax, Virginia
  • Local Institution - 6102Blacktown, New South Wales
  • Local Institution - 6103Heidelberg, Victoria
  • Local Institution - 6104Melbourne, Victoria
  • Local Institution - 6101Nedlands, Western Australia
  • Local Institution - 6303Seoul, Seoul-teukbyeolsi

Source and freshness
Processed from ClinicalTrials.gov. Last public update: May 26, 2023. Always confirm current availability with the study team.

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