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OncoMatch/Clinical Trials/NCT05873686

A Phase 1 Clinical Study of NXP900 in Subjects With Advanced Cancers

Is NCT05873686 recruiting? Yes, currently enrolling (Sep 2026). This Phase 1 trial studies NXP900 for advanced solid tumor.

Phase 1RecruitingNuvectis Pharma, Inc.NCT05873686Data as of Sep 2026Location: United States · United Kingdom

Treatment: NXP900This is a multi-center, first-in-human, open label, dose escalation (Part A) and expansion (Part B) Phase 1 study in subjects with advanced solid tumors and in subjects with solid tumors with selected genetic alterations that are either direct (YES1 amplification) or dependent (Hippo Pathway alterations) targets of NXP900.

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Extracted eligibility criteria

Treatments studied

Other

NXP900

Cancer type

Tumor Agnostic

Non-Small Cell Lung Carcinoma

Renal Cell Carcinoma

Mesothelioma

Biomarker criteria

Required: YES1 amplification

YES1 amplification (NSCLC adenocarcinoma or squamous cell carcinoma; other solid tumors)

Required: TYMS amplification

TYMS amplification (NSCLC adenocarcinoma or squamous cell carcinoma; other solid tumors)

Required: FAT1 pathogenic mutation

FAT1 pathogenic mutation (NSCLC adenocarcinoma or squamous cell carcinoma; other solid tumors)

Required: NF2 pathogenic mutation

NF2 pathogenic mutation (renal cancer, mesothelioma, other solid tumors)

Required: LATS1 pathogenic mutation

LATS1 pathogenic gene mutation (other solid tumors)

Required: YAP1 amplification

YAP1 gene amplification (other solid tumors)

Required: TAZ1 amplification

TAZ1 gene amplification (other solid tumors)

Required: IDH1 mutation

cholangiocarcinoma with IDH1 or IDH2 mutations

Required: IDH2 mutation

cholangiocarcinoma with IDH1 or IDH2 mutations

Excluded: HER2 (ERBB2) overexpression

Subjects with known human epidermal growth factor receptor 2 (HER2+) overexpressing malignancies

Excluded: BRAF mutation

Subjects with colorectal cancer, glioma, melanoma, or anaplastic thyroid conditions with BRAF mutations

Excluded: BRAF mutation

Subjects with NSCLC with BRAF or EGFR mutations or HER2 overexpression

Excluded: EGFR mutation

Subjects with NSCLC with BRAF or EGFR mutations or HER2 overexpression

Excluded: HER2 (ERBB2) overexpression

Subjects with NSCLC with BRAF or EGFR mutations or HER2 overexpression

Excluded: HER2 (ERBB2) alteration

Subjects with breast cancer, gastric cancer, esophageal junction adenocarcinoma or biliary cancer with HER2 alterations

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Max 3 prior lines
Min 1 prior line

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

US trial sites

  • Mayo Clinic · Phoenix, Arizona
  • UC San Diego Moores Cancer Center · La Jolla, California
  • Sarah Cannon Research Institute at HealthONE · Denver, Colorado
  • Mayo Clinic · Jacksonville, Florida
  • University of Chicago · Chicago, Illinois

Showing up to 5 US sites.

See all sites on ClinicalTrials.gov →

Frequently asked questions

Is NCT05873686 currently recruiting?

Yes, this trial is currently recruiting patients.

Does this trial require YES1?

Yes, YES1 amplification is a required biomarker for enrollment.

Does this trial require TYMS?

Yes, TYMS amplification is a required biomarker for enrollment.

Does this trial require FAT1?

Yes, FAT1 pathogenic mutation is a required biomarker for enrollment.

Are patients with ERBB2 alterations eligible?

No. ERBB2 overexpression is an exclusion criterion.

Are patients with BRAF alterations eligible?

No. BRAF mutation is an exclusion criterion.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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