[No standalone website (unbranded, no questionnaire)] A Study of Subjects With Psoriatic Arthritis to Investigate the Effectiveness of Adalimumab Introduction Compared With Methotrexate Dose Escalation (CONTROL)

How to apply

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Study’s contact

Call center

(858) 276-0005

Email address

clinical@tptherapeutics.com

Condition

ALK Gene Mutation,Advanced Solid Tumor,Metastatic Solid Tumor,NSCLC,Non Small Cell Lung Cancer,Non-Small Cell Lung Cancer

Treatment type

Interventional

Investigational product

TPX-0131

Phase

Phase 1/Phase 2

Sponsor

Turning Point Therapeutics, Inc.

ClinicalTrials.gov identifier

NCT04849273

Study number

TPX-0131-01

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About the study

A phase 1/2, 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). The study consists of two portions: 1) Phase 1 dose escalation, and 2) Phase 2 efficacy evaluation.

Who can take part?

You may be eligible to participate in the study if you meet the following criteria:

Inclusion criteria

  1. Age ≥ 18 (or as required by local regulation).
  2. Histological or cytological confirmation of advanced/metastatic ALK+ NSCLC.
  3. 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.
  4. ECOG performance status ≤ 1.
  5. Existence of measurable or evaluable disease (according to Response evaluation criteria in solid tumors [RECIST v1.1] criteria).
  6. Subjects with asymptomatic CNS metastases and/or asymptomatic leptomeningeal carcinomatosis are eligible.
  7. Adequate organ function.
Exclusion criteria

  1. Major surgery within four weeks of the start of TPX-0131 treatment.
  2. Clinically significant cardiovascular disease
  3. Any of the following cardiac criteria:
  4. 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
  5. Any clinically important abnormalities in rhythm, conduction, or morphology of resting ECG
  6. Known clinically significant active infections not controlled with systemic treatment (bacterial, fungal, viral including HIV positivity).
  7. Gastrointestinal disease or other malabsorption syndromes that would impact drug absorption.
  8. Subjects being treated with or anticipating the need for treatment with strong CYP3A4 inhibitors or inducers.
  9. Subjects with current or anticipated need for drugs that are sensitive CYP2C9 substrates with narrow therapeutic indices.

For a full list of inclusion/exclusion criteria, please visit ClinicalTrials.gov

Study locations

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How to apply

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