RecruitingPhase 1NCT06041516

A First-in-Human Phase I Trial With Antibody Drug Conjugate ADCT-701 in Neuroendocrine Tumors, Carcinomas and Malignant Peripheral Nerve Sheath Tumors


Sponsor

National Cancer Institute (NCI)

Enrollment

70 participants

Start Date

Jun 17, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

Background: Neuroendocrine neoplasms (NENs) are rare cancers in the gastrointestinal tract, pancreas, lungs, adrenal glands, and other areas of the body. Many of these cancers have a high risk of relapse and a low chance of survival. Better treatments are needed. Objective: To test a new drug, ADCT-701, in people with NENs. Eligibility: Adults aged 18 and older with NENs. Design: Participants will be screened. They will have a physical exam with blood and urine tests. They will have imaging scans and tests of heart functioning. Their ability to perform normal daily activities will be tested. A biopsy may be needed: A sample of tissue will be removed from the tumor. ADCT-701 is given through a tube attached to a needle inserted into a vein in the arm. Participants will receive the drug treatment on the first day of 21-day treatment cycles. They will visit the clinic a total of 10 times during the first two cycles. After that, they will visit the clinic 2 times during each cycle. Imaging scans, blood draws, heart function tests, and other tests will be repeated during study visits. Each visit will last up to 8 hours. Participants may continue receiving treatment with the study drug for up to 2 years. After treatment ends, participants will have follow-up clinic visits 4 times in 4 months. They will have a physical exam, with heart and blood tests, at each visit. After that, they will have follow-up clinic visits every 9 weeks; these visits will include imaging scans. Follow-up visits will continue for up to 5 years after treatment began....


Eligibility

Min Age: 18 YearsMax Age: 120 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a new antibody-drug conjugate called ADCT-701 — a targeted cancer drug that delivers chemotherapy directly to cancer cells — in patients with neuroendocrine tumors (slow- or fast-growing tumors that arise from hormone-producing cells) or adrenocortical carcinoma (cancer of the adrenal gland). **You may be eligible if...** - You have been confirmed to have a neuroendocrine tumor or adrenocortical carcinoma that has spread or cannot be removed - Your cancer has progressed after standard treatments or you cannot tolerate them - You are 18 or older with measurable disease on scans - Your blood counts and organ function are within acceptable ranges **You may NOT be eligible if...** - You have had recent blood transfusions or your blood counts are too low - You have active brain metastases or serious infections - You are pregnant or breastfeeding Talk to your doctor to see if this trial is right for you.

This is a simplified summary. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGADCT-701

ADCT-701 in 2microgram/kg-255microgram/kg (weight based dosing), IV over 30 minutes (+15 minutes)


Locations(1)

National Institutes of Health Clinical Center

Bethesda, Maryland, United States

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NCT06041516


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