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
What this study is about
- Purpose
- Treatment
- Study type
- Interventional
- Phase
- Phase 1
- Sponsor
- Turning Point Therapeutics, Inc.
- Interventions being studied
- Drug: TPX-0131
How this study is categorized
These labels come from structured fields and exact terms in the public record.
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.
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.