Phase 2 HIV and AIDS Trial, Recruiting NCT06445166 Sponsor: Washington University School of Medicine Condition: HIV and AIDS
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Phase 2 HIV and AIDS Trial, Recruiting

NCT06445166
Recruiting Phase 2

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who have a confirmed diagnosis of Kaposi Sarcoma (proven by biopsy) with lesions that can be measured with a ruler.
  • People who have either two lesions at least 4mm x 4mm in size, or one lesion at least 8mm x 8mm in size, that can be biopsied — plus at least 5 additional lesions elsewhere.
  • People aged 18 or older.
  • People who weigh at least 40 kg (approximately 88 pounds).
  • People who are reasonably able to carry out daily activities (a doctor will assess this using a standard scale called the ECOG scale, with a score of 2 or less required) (confirm with trial site).
  • People who are HIV-positive and have been on HIV treatment (antiretroviral therapy) for at least 12 weeks, meeting specific conditions about how long they have been on treatment and whether their Kaposi Sarcoma has been changing.
  • People who are HIV-negative and whose Kaposi Sarcoma has not been improving in the 12 weeks before joining the trial.
  • Women who could become pregnant must agree to use reliable contraception before, during, and for one month after taking part in the trial, and must report a suspected pregnancy to their treating doctor immediately.
  • People who are able to swallow an oral pill.
  • People who are willing and able to understand and sign a written consent form approved by an ethics review board.

Who may not be able to join:

  • People whose Kaposi Sarcoma has spread to internal organs in a way that is affecting how those organs function.
  • People who urgently need to start strong chemotherapy right away (though people who received chemotherapy more than 4 weeks before screening may still be considered).
  • People with another cancer (past or current) that could interfere with assessing how safe or effective the trial treatment is.
  • People who are currently taking a type of heart/blood pressure medication called beta-blockers for another condition (previous use may be allowed if stopped long enough before the trial starts — confirm with trial site).
  • People who are currently receiving any other cancer treatment, or who have received cancer treatment within the past 4 weeks.
  • People who are currently taking part in another clinical trial involving an investigational treatment.
  • People who have had an allergic reaction to propranolol or to medications with a similar chemical make-up.
  • People with a history of asthma, COPD, or other breathing airway conditions — though people with mild or well-controlled cases who have not had a flare-up requiring extra treatment in the past 3 months may still be considered.
  • People with a history of diabetes, as identified by specific blood sugar measurements (confirm with trial site for the specific values).
  • People with a history of heart failure that is not well managed, a very slow heart rate (persistently below 50 beats per minute), certain heart rhythm problems, or significant heart conduction issues — though people with a mildly slow but stable heart rate of at least 51 beats per minute and no symptoms may be considered.
  • People with a history of low blood pressure or significant drops in blood pressure when standing up — though isolated incidents may be discussed with the trial doctor.
  • People experiencing shortness of breath, coughing up blood, or a moderate to severe cough that cannot be explained by causes other than Kaposi Sarcoma — though those with minor, temporary symptoms and healthy oxygen levels may be considered.
  • People experiencing bleeding from the mouth or rectum that cannot be explained by causes other than Kaposi Sarcoma, unless it is minor and temporary (such as slight blood on toilet paper).
  • People with uncontrolled ongoing illness, such as a significant active infection, unstable heart conditions, or serious heart rhythm problems.
  • People currently showing signs of a serious condition called KSHV inflammatory cytokine syndrome (people with a past history of this condition may still be considered).
  • People who are pregnant or breastfeeding; women who could become pregnant must have a negative pregnancy test within 21 days of joining.
  • People with an untreated or inadequately treated active Hepatitis B virus (HBV) infection (those receiving HBV treatment or with an undetectable viral load on treatment may be considered; testing is not required unless there is a known history of infection).
  • People with a current or uncured Hepatitis C virus (HCV) infection with a detectable viral load (those who have been treated and cured, or who are on treatment with an undetectable viral load, may be considered; testing is not required unless there is a known history of infection).

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 12 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Lee Ratner, M.D., Ph.D., Washington University School of Medicine

Phone: 314-362-8836

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 2
Registry
ClinicalTrials.gov
Start date
20 August 2025
Est. completion
1 February 2028

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Objective response rate (ORR)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 12 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov