Recruiting
Phase 1
Phase 2

STX-721

Sponsor:

Pierre Fabre Medicament

Code:

NCT06043817

Conditions

Non-Small Cell Lung Cancer

NSCLC

EGFR/HER2 Exon 20 Insertion Mutation

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

STX-721/PFL-721 (Escalated)

STX-721/PFL-721 (3 dose levels)

STX-721/PFL-721 (RP2D)

Study Details

Brief 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.

Conditions

Non-Small Cell Lung Cancer

NSCLC

EGFR/HER2 Exon 20 Insertion Mutation

Study ID

NCT06043817

Start date

Sep 26, 2023

Status verified date

Aug, 2026

Completion date

Dec 1, 2029

Anticipated

Primary completion date

Dec 1, 2029

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

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

345 participants

Anticipated

Allocation

Non randomized

Intervention Model

Sequential

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Part 1: Dose Escalation

experimental: Part 2: RP2D Selection

experimental: Part 3: Dose Expansion

Interventions

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.

Primary outcome measure

  • 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 ]

Central Contacts and Locations

Central contacts

Adele De MASSON, clinical devlopment director, MD, PhD

33 772344916PFL721_medical.team@pierre-fabre.com

Locations

City of Hope

Recruiting

Duarte, California, United States, 91010

City of Hope

Recruiting

Huntington Beach, California, United States, 92648

City of Hope

Recruiting

Irvine, California, United States, 92618

Levine Cancer Institute - Charlotte

Recruiting

Charlotte, North Carolina, United States, 28204-2990

Thomas Jefferson University Research Facility

Recruiting

Philadelphia, Pennsylvania, United States, 19107

SCRI Oncology Partners - PPDS

Recruiting

Nashville, Tennessee, United States, 37203

University of Texas MD Anderson Cancer Center

Recruiting

Houston, Texas, United States, 77030-4009

University of Utah - Huntsman Cancer Institute - PPDS

Recruiting

Salt Lake City, Utah, United States, 84112-5550

NEXT Virginia

Recruiting

Fairfax, Virginia, United States, 22031-2171

More Information

Sponsor

Pierre Fabre Medicament

Last update posted

Sep 2, 2026

Last verified

Aug, 2026

Keywords

  • Exon 20, EGFR, HER2, NSCLC, TKI

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-08. This information was provided to ClinicalTrials.gov by Pierre Fabre Medicament on 2026-09-02.