RecruitingPhase 2NCT06445166

Propranolol for the Treatment of Kaposi Sarcoma in Adults

A Multicenter Phase II Study of Propranolol for the Treatment of Kaposi Sarcoma in Adults


Sponsor

Washington University School of Medicine

Enrollment

25 participants

Start Date

Aug 20, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

Kaposi sarcoma (KS) lesions are initiated by endothelial cells infected with KS herpesvirus (KSHV), also known as human herpesvirus 8 (HHV-8). Lesion progression is driven by abnormal angiogenesis, chronic inflammation, and uncontrolled cell proliferation. KS remains one of the most commonly diagnosed cancers in many African countries where economic constraints prevent successful treatment in most patients. Treatment outcomes in developed countries are also often unsatisfactory in HIV positive patients despite good virological and immunological responses to antiretroviral therapy. Therefore, identification of new oral, safe treatment options for treatment of KS remains a research priority. Given the known anti-angiogenic properties and based on the treatment response with other benign vascular lesions such as infantile hemangioma, propranolol is a good candidate for the treatment of KS. The hypothesis of this study is that treating patients with Kaposi sarcoma with propranolol will result in an overall response rate (complete response rate plus partial response rate) of at least 45%, and that propranolol will be safe and well tolerated in this patient population.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study tests whether propranolol — a common heart medication called a beta-blocker — can treat Kaposi sarcoma (KS), a type of cancer that causes skin lesions and can affect internal organs. KS is often found in people with HIV. **You may be eligible if...** - You are 18 or older and weigh at least 40 kg - You have Kaposi sarcoma confirmed by biopsy, with enough measurable skin lesions - If HIV-positive, you have been on antiretroviral therapy for at least 12 weeks - You are able to swallow pills and give informed consent **You may NOT be eligible if...** - Your Kaposi sarcoma is affecting internal organs and causing significant problems - You need urgent chemotherapy right away - You have asthma or COPD (chronic lung disease) - You have diabetes - You have a history of serious heart problems (heart failure, low blood pressure, significant heart block) - You are pregnant or breastfeeding - You are currently taking another beta-blocker medication 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

DRUGPropranolol Hydrochloride

Dosing is as follows: * Patients who weigh 40 to 59.9 kg: * 40 mg BID (target) * 20 mg BID (half the target) * Patients who weigh ≥ 60 kg: * 60 mg BID (target) * 30 mg BID (half the target)


Locations(1)

Washington University School of Medicine

St Louis, Missouri, United States

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NCT06445166


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