Study STX-721-101/PFL-721CI101 is an open label, Phase 1/2 study evaluating the safety, tolerability, pharmacokinetic (PK) exposure, and preliminary antitumor activity of STX-721/PFL-721 in participants with non-small cell lung cancer (NSCLC) carrying EGFR or HER2 exon 20 insertion (ex20ins) mutations.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
251
STX-721/PFL-721 dose will be escalated per cBLRM-design.
Participants will receive STX-721/PFL-721 at one of three dose levels.
Participants will receive the RP2D of STX-721/PFL-721.
City of Hope
Duarte, California, United States
RECRUITINGCity of Hope
Huntington Beach, California, United States
RECRUITINGCity of Hope
Irvine, California, United States
RECRUITINGLevine Cancer Institute - Charlotte
Charlotte, North Carolina, United States
RECRUITINGThomas Jefferson University Research Facility
Philadelphia, Pennsylvania, United States
RECRUITINGSCRI Oncology Partners - PPDS
Nashville, Tennessee, United States
RECRUITINGUniversity of Texas MD Anderson Cancer Center
Houston, Texas, United States
RECRUITINGUniversity of Utah - Huntsman Cancer Institute - PPDS
Salt Lake City, Utah, United States
RECRUITINGNEXT Virginia
Fairfax, Virginia, United States
RECRUITINGEDOG Institut de Cancerologie de l'Ouest - PPDS
Saint-Herblain, Loire-Atlantique, France
RECRUITING...and 13 more locations
Part 1 Dose Escalation (MTD): Dose Escalation - Number of participants who experience at least 1 DLT during the first 28 days of treatment
Time frame: 28 days
Part 1 Dose Escalation (OBD): Dose Escalation - Number of participants who experience at least 1 DLT during the first 28 days of treatment
Time frame: 28 days
Part 2 RP2D Selection: C(max) of STX-721/PFL-721
Time frame: 1 year
Part 2 RP2D Selection: AUC(0-inf) of STX-721/PFL-721
Time frame: 1 year
Part 2 RP2D Selection: AUC(0-t) of STX-721/PFL-721
Time frame: 1 year
Part 2 RP2D Selection: AUC(0-τ) of STX-721/PFL-721
Time frame: 1 year
Part 2 RP2D Selection: Number of participants with confirmed objective response rate (ORR) defined as the percentage of participants with partial response (PR) or complete response (CR) based on RECIST v1.1 per investigator assessment.
Time frame: 1 year
Part 3 Dose Expansion: Number of participants with confirmed ORR defined as the percentage of participants with PR or CR based on RECIST v1.1 per investigator assessment.
Time frame: 1 year
Claire FABRE, Head of clinical development, MD, PhD
CONTACT
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