Phase III Study of TY-9591 in Patients With Locally Advanced or Metastatic Non-small Cell Lung Cancer (FLETEO)

Sponsor
TYK Medicines, Inc
Study ID
NCT05382728
Phase
PHASE3
Status
Recruiting

Conditions

  • EGFR Activating Mutation
  • NSCLC

Eligibility Criteria

Sex
ALL
Age
18 Years - 80 Years
Healthy Volunteers
Not accepted

Interventions

  • TY-9591 — DRUG
    The dose of TY-9591 is 160 mg once daily. A cycle of treatment is defined as 21 days of once daily treatment. Number of Cycles: as long as patients are continuing to show clinical benefit, as judged by the Investigator, and in the absence of discontinuation criteria.
  • placebo Osimertinib — DRUG
    The dose of placebo Osimertinib is 80 mg once daily. A cycle of treatment is defined as 21 days of once daily treatment. Number of Cycles: as long as patients are continuing to show clinical benefit, as judged by the Investigator, and in the absence of discontinuation criteria.
  • Osimertinib — DRUG
    The dose of Osimertinib is 80 mg once daily. A cycle of treatment is defined as 21 days of once daily treatment. Number of Cycles: as long as patients are continuing to show clinical benefit, as judged by the Investigator, and in the absence of discontinuation criteria.
  • placebo TY-9591 — DRUG
    The dose of placebo TY-9591 is 160 mg once daily. A cycle of treatment is defined as 21 days of once daily treatment. Number of Cycles: as long as patients are continuing to show clinical benefit, as judged by the Investigator, and in the absence of discontinuation criteria.

Study Details

To assess the efficacy and safety of TY-9591 versus Osimertinib in patients with locally advanced or Metastatic Non Small Cell Lung Cancer.

Key Dates

Start date
Jun 8, 2022
Status verified
Jan 2024
Primary completion
May 31, 2025
Completion
Dec 31, 2027

Study Design

Enrollment
680 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: TY-9591+placebo Osimertinib
    TY-9591 (160mg orally, once daily) plus placebo Osimertinib (80mg orally, once daily), in accordance with the randomization schedule.
  • Active Comparator: Osimertinib+placebo TY-9591
    Osimertinib (80mg orally, once daily) plus placebo TY-9591 (160mg orally, once daily), in accordance with the randomization schedule.

Primary Outcome Measure

Median Progression Free Survival (PFS) [ Time Frame: approximately 18 months ]

Central Contacts

Related coverage on Hipa.ai

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