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OncoMatch/Clinical Trials/NCT05552781

H002 in Patients With EGFR Mutation Locally Advanced or Metastatic NSCLC

Is NCT05552781 recruiting? Yes, currently enrolling (May 2026). This Phase 1/2 trial studies H002 capsule for non-small cell lung cancer.

Phase 1/2RecruitingRedCloud BioNCT05552781Data as of May 2026

Treatment: H002 capsuleThis is a phase I/IIa, open-label, dose-escalation and expansion study to evaluate the safety, tolerability, PK and preliminary anti-tumor activity of H002 when given orally in patients with EGFR mutation-positive locally advanced or metastatic non-small cell lung cancer (NSCLC). The study will contain two parts: Part A is dose escalation phase (i.e., Phase I) and Part B is dose expansion phase (i.e., Phase IIa).

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Extracted eligibility criteria

Cancer type

Non-Small Cell Lung Carcinoma

Biomarker criteria

Required: EGFR activating mutation

NSCLC harboring one or more active EGFR mutations known to be associated with EGFR-TKI sensitivity (including, but not limited to Del19 and L858R)

Required: EGFR exon 19 deletion

including, but not limited to Del19 and L858R

Required: EGFR L858R

including, but not limited to Del19 and L858R

Required: EGFR C797S

subjects must have NSCLC harboring EGFR C797S mutation (Part B)

Excluded: EGFR exon 20 insertion

Subjects with EGFR exon 20 insertion mutations only

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Must have received: EGFR tyrosine kinase inhibitor

Subjects have received at least one previous EGFR-TKI treatment and have radiological documented disease progression on the previous continuous EGFR-TKI treatment (Part B)

Cannot have received: EGFR tyrosine kinase inhibitor

Exception: washout required: 8 days or approximately 5 × t1/2 prior to first dose of H002, whichever is longer

Prior treatment with an EGFR-TKI within 8 days or approximately 5 × t1/2 prior to the first dose of H002, whichever is longer

Cannot have received: immunotherapy or biotherapy

Exception: washout required: 4 weeks prior to first dose of H002

Prior treatment with immunotherapy or biotherapy within 4 weeks prior to the first dose of H002

Cannot have received: radiation therapy

Exception: palliative radiotherapy completed at least 2 weeks prior to first dose of H002 can be enrolled

Radiotherapy (palliative radiotherapy is completed at least 2 weeks prior to the first dose of H002 can be enrolled) within 4 weeks prior to the first dose of H002

Cannot have received: herbal therapy with anti-tumor effects

Exception: washout required: 2 weeks prior to first dose of H002

Herbal therapy that has anti-tumor effects within 2 weeks prior to the first dose of H002

Cannot have received: mitomycin (mitomycin)

Exception: washout required: 6 weeks prior to first dose of H002

Mitomycin and nitrosourea within 6 weeks prior to the first dose of H002

Cannot have received: nitrosourea (nitrosourea)

Exception: washout required: 6 weeks prior to first dose of H002

Mitomycin and nitrosourea within 6 weeks prior to the first dose of H002

Cannot have received: oral fluorouracil (tegafur, capecitabine)

Exception: washout required: 2 weeks prior to first dose of H002

Oral fluorouracil such as tegafur and capecitabine within 2 weeks prior to the first dose of H002

Cannot have received: chemotherapy

Exception: except for mitomycin, nitrosourea, and fluorouracil oral drugs; washout required: 4 weeks or approximately 5 × t1/2 prior to first dose of H002, whichever is longer

Chemotherapy (except for mitomycin, nitrosourea, and fluorouracil oral drugs), or other anti-tumor drugs for the treatment of NSCLC within 4 weeks or approximately 5 × t1/2 prior to the first dose of H002, whichever is longer

Cannot have received: EGFR C797S-targeted therapy (BTP-661411, TQB3804, BLU-945)

Prior marketed and/or investigational treatment for EGFR C797S mutation (including, but not limited to BTP-661411, TQB3804 and BLU-945)

Lab requirements

Blood counts

Adequate hematologic function per protocol

Kidney function

Adequate organ function per protocol

Liver function

Adequate organ function per protocol

Adequate hematologic and organ function per protocol

Structured fields extracted by AI. May contain errors — verify against the official protocol.

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