RecruitingRecruiting
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
NCT06043817 · Pierre Fabre Medicament
In plain English
Click the button to translate this study into plain language — what it is, who qualifies, and what participation looks like.
About this study
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 criteria
Key Inclusion Criteria:
1. Has histologically- or cytologically confirmed diagnosis of NSCLC Stage IIIB/C or IV not eligible for curative intent surgery or chemoradiation
2. Part 1: Tumor tissue EGFR or HER2 exon 20 insertion mutations confirmed by qualified local laboratories. Parts 2 and 3: EGFR/HER2 exon 20 insertion mutations confirmed by qualified local laboratories
3. Part 1: Has received all approved therapies for advanced or metastatic NSCLC or is ineligible. Part 2 and Part 3: Has received at least 1, but not more than 2, prior lines of approved treatment for advanced or metastatic NSCLC, 1 of which must be platinum-based chemotherapy unless contraindicated
4. Has documented tumor progression (based on radiological imaging)
5. Has new or recent tumor biopsy (collected at screening, if feasible) or archival tumor specimen collected in the past 10 years available for genomic profiling
6. Has at least one measurable tumor lesion per RECIST v1.1
7. Is ≥18 years of age at the time of signing the ICF
8. Has Eastern Cooperative Oncology Group (ECOG) performance status score of 0 or 1
Key Exclusion Criteria:
1. Has a tumor that is known to harbor EGFR ex20ins p.H773\_V774insH variant, or any EGFR kinase domain activating mutation concurrent with either a T790M and/or C797S resistance mutations
2. Has history (within ≤2 years before screening) of solid tumor or hematological malignancy that is histologically distinct from NSCLC
3. Has symptomatic brain or spinal metastases
4. Has toxicities from previous anticancer therapies that have not resolved to baseline levels or to CTCAE Grade ≤1, except for alopecia and peripheral neuropathy
5. Has any condition for which, in the opinion of the investigator, participation would not be in the best interest of the participant (e.g., could compromise the participant's well-being) or would prevent, limit, or confound the protocol-specified assessments
Study design
Enrollment target: 345 participants
Allocation: non_randomized
Masking: none
Age groups: adult, older_adult
Timeline
Starts: 2023-09-26
Estimated completion: 2029-12-01
Last updated: 2026-05-22
Interventions
Drug: STX-721/PFL-721 (Escalated)Drug: STX-721/PFL-721 (3 dose levels)Drug: STX-721/PFL-721 (RP2D)
Primary outcomes
- • 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)
Sponsor
Pierre Fabre Medicament · industry
Contacts & investigators
ContactAdele De MASSON, clinical devlopment director, MD, PhD · contact · PFL721_medical.team@pierre-fabre.com · 33 772344916
All locations (24)
City of HopeRecruiting
Duarte, California, United States
City of HopeRecruiting
Huntington Beach, California, United States
City of HopeRecruiting
Irvine, California, United States
Levine Cancer Institute - CharlotteRecruiting
Charlotte, North Carolina, United States
Thomas Jefferson University Research FacilityRecruiting
Philadelphia, Pennsylvania, United States
SCRI Oncology Partners - PPDSRecruiting
Nashville, Tennessee, United States
University of Texas MD Anderson Cancer CenterRecruiting
Houston, Texas, United States
University of Utah - Huntsman Cancer Institute - PPDSRecruiting
Salt Lake City, Utah, United States
NEXT VirginiaRecruiting
Fairfax, Virginia, United States
EDOG Institut de Cancerologie de l'Ouest - PPDSRecruiting
Saint-Herblain, Loire-Atlantique, France
Institut Claudius Regaud - PPDSRecruiting
Toulouse, France
Gustave RoussyRecruiting
Villejuif, France
Charité - Universitätsmedizin Berlin (CBF) - Hindenburgdamm 30Recruiting
Berlin, Germany
Universitätsklinikum Carl Gustav Carus an der TU DresdenRecruiting
Dresden, Germany
Nederlands Kanker Instituut-Antoni van Leeuwenhoek ZiekenhuisRecruiting
Amsterdam, Netherlands
Chungbuk National University HospitalRecruiting
Cheongju-si, South Korea
CHA Bundang Medical Center, CHA UniversityRecruiting
Seongnam-si, South Korea
Seoul National University HospitalRecruiting
Seoul, South Korea
Hospital Regional Universitario de Malaga - Hospital GeneralRecruiting
Málaga, Malaga, Spain
Instituto de Investigacion Oncologica Vall dHebron (VHIO) - EPONRecruiting
Barcelona, Spain
Hospital Universitario Ramon y CajalRecruiting
Madrid, Spain
Hospital Universitario Virgen del RocioRecruiting
Seville, Spain
National Taiwan University HospitalRecruiting
Taipei, Taiwan
Taipei Veterans General HospitalRecruiting
Taipei, Taiwan