RecruitingPhase 1Phase 2NCT04303117

PDS01ADC Monotherapy and in Combination With M7824 in Advanced Kaposi Sarcoma

Phase I/II Study of PDS01ADC Monotherapy and in Combination With M7824 in Advanced Kaposi Sarcoma


Sponsor

National Cancer Institute (NCI)

Enrollment

80 participants

Start Date

Jul 13, 2020

Study Type

INTERVENTIONAL

Conditions

Summary

Background: Kaposi sarcoma (KS) tumors grow on the skin, lymph nodes, lungs, bone, and gastrointestinal tract. KS often affects people with immune deficiencies, such as among people living with HIV or those with prior history of transplant. Researchers want to see if 2 non-chemotherapy drugs can help people with KS. PDS01ADC triggers the immune system to fight tumors. M7824 blocks the pathways that cancer cells use to stop the immune system from fighting tumors. Objective: To learn if giving PDS01ADC alone or with M7824 could help the immune system fight KS tumors. Eligibility: People 18 and older with KS that has been treated with chemotherapy or immunotherapy Design: Participants will be screened with some or all of the following: medical history physical exam chest X-ray computed tomography scan blood and urine tests electrocardiogram and echocardiogram skin KS lesion biopsy lung exam gastrointestinal exam All participants will get PDS01ADC every 4 weeks for up to 96 weeks (or 24cycles). It is injected under the skin. Some participants will also get M7824 every 2 weeks for up to 96 weeks (or 24cycles). It is given through a plastic tube that is put in an arm vein. Participants will complete questionnaires about how KS affects their quality of life. Their KS lesions will be measured and photographed. They will repeat some of the screening tests. They will give saliva samples or additional tissue samples. They will have a lung function test. Their ability to perform their normal activities will be assessed. The treatment duration is up to 96 weeks (or 24cycles) with an option to take PDS01ADC and/or M7824 until the KS tumors are not responding, or you develop unacceptable side effects. Participants will have follow-up visits 7 and 30 days after treatment ends, then every 3 to 6 months for the next 18 months, then once a year for 3 years.


Eligibility

Min Age: 18 YearsMax Age: 99 Years

Plain Language Summary

Simplified for easier understanding

This study is testing two experimental treatments — NHS-IL12 (a drug that activates the immune system) alone and in combination with M7824 (a drug that removes 'brakes' from the immune system) — to treat Kaposi sarcoma, a cancer that causes lesions on the skin and internal organs, often in HIV-positive individuals. **You may be eligible if...** - You have confirmed Kaposi sarcoma - Your Kaposi sarcoma is widespread, affecting quality of life, or has not responded to prior treatments (like chemotherapy or immunotherapy) - You have completed a washout period from prior treatments - Your organ function (blood, liver, kidneys) meets minimum requirements **You may NOT be eligible if...** - You have untreated or unstable HIV (if HIV-positive, virus must be well-controlled on medication) - You have severe autoimmune disease - You have active, serious infections - You are pregnant or breastfeeding - You have had recent major surgery Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGPDS01ADC

An initial dose of 16.8 mcg/kg administered subcutaneously every 4 weeks and at an MTD dose with M7824 on day 1 of a 28-day cycle.

DRUGM7824

1200 mg administered IV every two weeks while on PDS01ADC.


Locations(1)

National Institutes of Health Clinical Center

Bethesda, Maryland, United States

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NCT04303117


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