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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.

Phase 1RecruitingNextCure, Inc.NCT06774963Data as of May 2026

Treatment: LNCB74This 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.

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Extracted 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 →

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