OncoMatch/Clinical Trials/NCT06774963
A Phase 1 Study of LNCB74 in Advanced Solid Tumors
Is NCT06774963 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies LNCB74 for ovarian cancer.
Treatment: LNCB74 — This is an open-label, phase 1, dose escalation and dose expansion study to determine safety and tolerability, and to determine the maximum tolerated dose and / or recommended phase 2 dose of LNCB74 in participants with advanced solid tumors.
Check if I qualifyExtracted eligibility criteria
Cancer type
Ovarian Cancer
Breast Carcinoma
Endometrial Cancer
Cholangiocarcinoma
Non-Small Cell Lung Carcinoma
Tumor Agnostic
Disease stage
Metastatic disease required
Performance status
ECOG 0–1(Restricted strenuous activity)
Prior therapy
Cannot have received: investigational agent
Has received prior investigational agents within 4 weeks prior to treatment.
Cannot have received: immunotherapy (non-antibody-based therapy)
Has received anti-cancer chemotherapy (Immunotherapy (non-antibody-based therapy), retinoid therapy, hormonal therapy within 2 weeks prior to treatment.
Cannot have received: retinoid therapy
Has received anti-cancer chemotherapy (Immunotherapy (non-antibody-based therapy), retinoid therapy, hormonal therapy within 2 weeks prior to treatment.
Cannot have received: hormonal therapy
Has received anti-cancer chemotherapy (Immunotherapy (non-antibody-based therapy), retinoid therapy, hormonal therapy within 2 weeks prior to treatment.
Cannot have received: antibody-based anti-cancer therapy
Has received antibody-based anti-cancer therapy within 4 weeks prior to treatment.
Cannot have received: targeted agents and small molecules
Has received targeted agents and small molecules within 2 weeks or 5 half-lives, whichever is longer.
Cannot have received: platinum-based chemotherapy
Exception: progressed within 4 weeks of initiating therapy (platinum-refractory disease)
Has received prior platinum-based chemotherapy and progressed within 4 weeks of initiating therapy (platinum-refractory disease)
Cannot have received: antibody-drug conjugate
Exception: ADC with MMAE payload
Has received an ADC with MMAE payload.
Cannot have received: radiation therapy
Exception: focal radiation within 2 weeks or wide-field radiotherapy within 4 weeks
Has received prior radiotherapy within 2 weeks of start of study treatment for focal radiation or within 4 weeks for wide-field radiotherapy
Lab requirements
Blood counts
adequate organ function
Kidney function
adequate organ function
Liver function
adequate organ function
Have adequate organ function
Structured fields extracted by AI. May contain errors — verify against the official protocol.
US trial sites
- Hoag Family Cancer Institute · Newport Beach, California
- St. Elizabeth Healthcare · Edgewood, Kentucky
- Dana Farber Cancer Institute · Boston, Massachusetts
- Washington University, Siteman Cancer Center · St Louis, Missouri
- John Theurer Cancer Ctr at Hackensack Univ. Med Ctr. · Hackensack, New Jersey
Showing up to 5 US sites. See all sites on ClinicalTrials.gov →
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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