First-In-Human Study of STX-721/PFL-721 in Participants With Locally Advanced or Metastatic Non-Small Cell Lung Cancer Harboring EGFR or HER2 Exon 20 Insertion Mutations
Condition(s) studied
Investigational drug(s) / intervention(s)
STX-721/PFL-721 (Escalated): STX-721/PFL-721 dose will be escalated per cBLRM-design.
STX-721/PFL-721 (3 dose levels): Participants will receive STX-721/PFL-721 at one of three dose levels.
STX-721/PFL-721 (RP2D): Participants will receive the RP2D of STX-721/PFL-721.
Study summary
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.
Eligibility
Primary outcome measure(s)
- Part 1 Dose Escalation (MTD): Dose Escalation - Number of participants who experience at least 1 DLT during the first 28 days of treatment — 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 — 28 days
- Part 2 RP2D Selection: C(max) of STX-721/PFL-721 — 1 year
- Part 2 RP2D Selection: AUC(0-inf) of STX-721/PFL-721 — 1 year
- Part 2 RP2D Selection: AUC(0-t) of STX-721/PFL-721 — 1 year
- Part 2 RP2D Selection: AUC(0-τ) of STX-721/PFL-721 — 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. — 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. — 1 year
Trial sites (25)
| Facility | City | Region | Status |
|---|---|---|---|
| City of Hope | Duarte | California | Recruiting |
| City of Hope | Huntington Beach | California | Recruiting |
| City of Hope | Irvine | California | Recruiting |
| Levine Cancer Institute - Charlotte | Charlotte | North Carolina | Recruiting |
| Thomas Jefferson University Research Facility | Philadelphia | Pennsylvania | Recruiting |
| SCRI Oncology Partners - PPDS | Nashville | Tennessee | Recruiting |
| University of Texas MD Anderson Cancer Center | Houston | Texas | Recruiting |
| University of Utah - Huntsman Cancer Institute - PPDS | Salt Lake City | Utah | Recruiting |
| NEXT Virginia | Fairfax | Virginia | Recruiting |
| EDOG Institut de Cancerologie de l'Ouest - PPDS | Saint-Herblain | Loire-Atlantique | Recruiting |
| Institut Claudius Regaud - PPDS | Toulouse | France | Recruiting |
| Gustave Roussy | Villejuif | France | Recruiting |
| Charité - Universitätsmedizin Berlin (CBF) - Hindenburgdamm 30 | Berlin | Germany | Recruiting |
| Universitätsklinikum Carl Gustav Carus an der TU Dresden | Dresden | Germany | Recruiting |
| Nederlands Kanker Instituut-Antoni van Leeuwenhoek Ziekenhuis | Amsterdam | Netherlands | Recruiting |
| Chungbuk National University Hospital | Cheongju-si | South Korea | Recruiting |
| CHA Bundang Medical Center, CHA University | Seongnam-si | South Korea | Recruiting |
| Seoul National University Hospital | Seoul | South Korea | Recruiting |
| START - Rioja Hospital Universitario San Pedro | Logroño | La Rioja | Recruiting |
| Hospital Regional Universitario de Malaga - Hospital General | Málaga | Malaga | Recruiting |
| Instituto de Investigacion Oncologica Vall dHebron (VHIO) - EPON | Barcelona | Spain | Recruiting |
| Hospital Universitario Ramon y Cajal | Madrid | Spain | Recruiting |
| Hospital Universitario Virgen del Rocio | Seville | Spain | Recruiting |
| National Taiwan University Hospital | Taipei | Taiwan | Recruiting |
| Taipei Veterans General Hospital | Taipei | Taiwan | Recruiting |
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This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06043817 on ClinicalTrials.gov ↗ ← All trials in South Korea