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OncoMatch/Clinical Trials/NCT06380816

A Phase I/II Trial of UCB4594 in Participants With Advanced Cancer

Is NCT06380816 recruiting? Yes, currently enrolling (May 2026). This Phase 1/2 trial studies UCB4594 for advanced solid tumours.

Phase 1/2RecruitingCancer Research UKNCT06380816Data as of May 2026

Treatment: UCB4594This clinical trial is looking at UCB4594. This is the first time the drug is being tested in humans. UCB4594 is a type of drug called a monoclonal antibody. It has been designed to work by targeting a protein called human leucocyte antigen G (HLA-G) that is found in high levels on some cancer cells. By attaching itself to this protein it may help the immune system to attack and kill the cancer cells. The four main aims of the clinical trial are to find out: 1. The best dose of UCB4594 that can be given safely to participants in the trial. 2. What the side effects of UCB4594 are and how they can be managed. 3. What happens to UCB4594 inside the body and how it affects cancer cells. 4. Whether UCB4594 can cause cancer to shrink.

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Extracted eligibility criteria

Cancer type

Head and Neck Squamous Cell Carcinoma

Non-Small Cell Lung Carcinoma

Colorectal Cancer

Triple-Negative Breast Cancer

Breast Carcinoma

Renal Cell Carcinoma

Esophageal Carcinoma

Gastrointestinal Stromal Tumor

Gastric Cancer

Cervical Cancer

Ovarian Cancer

Pancreatic Cancer

Biomarker criteria

Required: HLA-G overexpression (high levels (as reported in the literature))

Tumour types which have shown high levels of human HLA-G expression (as reported in the literature)

Disease stage

Metastatic disease required

advanced solid tumours (as specified below), refractory to conventional treatment, or for which no conventional therapy is considered appropriate by the Investigator or is declined by the participant

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Must have received: conventional treatment

refractory to conventional treatment, or for which no conventional therapy is considered appropriate by the Investigator or is declined by the participant

Cannot have received: HLA-G, ILT2 or ILT4-targeting drug

Prior treatment with HLA-G, immunoglobulin-like transcript (ILT)2 or ILT4-targeting drug

Lab requirements

Blood counts

haematological indices within defined ranges

Kidney function

biochemical indices within defined ranges

Liver function

biochemical indices within defined ranges

Haematological and biochemical indices within defined ranges. These measurements should be performed to confirm the patient's eligibility to participate in the trial

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

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