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NCT07566494 · ClinicalTrials.gov registry record · Phase 1

Escalating Doses of VAS-101 in Subjects With Stable Sickle Cell Disease

A Phase 1 study, sponsored by National Heart, Lung, and Blood Institute (NHLBI).

Recruiting
Registry status
Phase 1
Development phase
25
Enrollment target

NCT07566494: Recruiting Phase 1 study, sponsored by National Heart, Lung, and Blood Institute (NHLBI).

NCT07566494 is a Phase 1 study that is actively recruiting participants, run by National Heart, Lung, and Blood Institute (NHLBI). The registered enrollment target is 25 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (58% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07566494, a Phase 1 study, is actively recruiting participants, sponsored by National Heart, Lung, and Blood Institute (NHLBI).

RECRUITING
Registry status
Phase 1
Development phase
25 participants
Enrollment target

Study Summary

Background: Sickle cell disease (SCD) is an inherited blood disorder. The disease affects the ability of red blood cells to carry oxygen. Research has shown that curcumin, a natural compound found in turmeric, can improve the health of red blood cells in people with SCD. But the body cannot absorb curcumin well when it is taken by mouth. Researchers want to know if a skin gel (VAS-101) can help the body better absorb curcumin. VAS-101 contains curcumin, which comes from turmeric. Objective: To test VAS-101 in people with stable SCD. Eligibility: People aged 18 to 70 years with stable SCD. Design: People who want to join the study will be screened with physical exam with blood tests to see if they are eligible. If they qualify, they can enroll in the study. Participants will have up to 15 clinic visits over about 14 weeks. Some may need to stay overnight in the hospital for up to 2 days to make it easier to collect blood samples after the gel is applied. For 6 weeks, a special gel called VAS-101 will be put on the forearms in the clinic two times a week. Staff will rub the gel into the skin for at least 30 seconds using a soft toothbrush. The area stays uncovered for at least 10 minutes, then is covered with a bandage or sleeve. After 24 hours, the dressing can be removed and the skin can be washed. Some visits will include blood tests and other exams. On three visits, a test called near infrared spectroscopy (NIRS) will be done. For this test, probes are placed on the skin to measure blood flow, oxygen levels, and the makeup of skin and muscle. A blood pressure cuff is used to squeeze the arm for up to 5 minutes. The last clinic visit will happen about 4 weeks after the final gel application....

Primary Outcome

-To evaluate the safety and tolerability of VAS-101 as assessed by:-The type, incidence, severity, and relationship to study treatment of AEs and serious adverse events (SAEs) from Baseline to Day 66, including:-Number of most common treatment related adverse events-Number of serious adverse events possibly related to treatment-Number of discontinuations due to AEs from Baseline to Day 66-Mean change in clinical laboratory test results (e.g., serum chemistry, liver function test, hematology, coa

Interventions

  • DRUG VAS-101

Trial Details

FieldValue
Enrollment Target 25 participants
Start Date 2026-07-15
Est. Completion 2027-04-27
Phase Phase 1

What NCT07566494 shows while recruiting

NCT07566494 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 25 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (58% lower).

The record links to 0 conditions, and to 1 intervention - of which VAS-101 is the first listed.

NCT07566494 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07566494 about?

NCT07566494 is a clinical study titled "Escalating Doses of VAS-101 in Subjects With Stable Sickle Cell Disease". Background: Sickle cell disease (SCD) is an inherited blood disorder. The disease affects the ability of red blood cells to carry oxygen. Research has shown that curcumin, a natural compound found in turmeric, can improve the health of red blood cells in people with SCD. But the body cannot absorb ...

What is the current status of trial NCT07566494?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 25 participants. The study started on 2026-07-15. Estimated completion is 2027-04-27.

What interventions are being tested in trial NCT07566494?

The interventions under investigation include: VAS-101 (DRUG).

Who is sponsoring clinical trial NCT07566494?

This trial is sponsored by National Heart, Lung, and Blood Institute (NHLBI), which has 501 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT07566494's enrollment target sits among peer trials

25 1495th of 2000 higher than 481 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT07566494, the US trial registry maintained by the National Library of Medicine. NCT07566494 (small enrollment · none site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.