Healthy Adult Subjects

5

Review clinical trials related to Healthy Adult Subjects. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Mass Balance Study of [14C]DA-302168S in Healthy Chinese Adult Male Participants

In this study, a single dose of \[14C\] radiolabelled DA-302168S will be administered orally. The main purpose of this study is to find out how much of DA-302168S and its metabolites pass from blood into urine and feces, and characterize the metabolic profile and routes of excretion of oral \[14C\] DA-302168S.

Participants needed: 10
Trial details
Phase: Phase 1Age: 18-55Biological sex: MaleType: InterventionalSponsor: Chendu DIAO Pharmaceutical Group CO., LTD.Updated: Oct 5, 2026
Eligibility criteria

History or family history of medullary thyroid carcinoma, thyroid C-cell hyperpl...

Status: Recruiting

PSTC100 Study in Healthy Adult Subjects

This study is a single-center, randomized, double-blind, placebo-controlled, dose-escalation phase I clinical trial designed to evaluate the safety, tolerability, pharmacokinetic, and pharmacodynamic (PD) characteristics of PSTC100 in healthy adult subjects.

Participants needed: 70
Trial details
Phase: Phase 1Age: 18-55Biological sex: AllType: InterventionalSponsor: Prospect Therapeutics (Nanjing) LimitedUpdated: Sep 4, 2026Locations: 1
Eligibility criteria

1.Fully understand the purpose and process of this study, voluntarily participat... [+6]

1.Pregnant women (or those with a positive pregnancy test), or breastfeeding wom... [+17]

Status: Recruiting

PSTB100 Study in Healthy Adult Subjects

This study is a randomized, double-blind, placebo-controlled, dose-escalation, first-in-human clinical trial in healthy adults, designed to assess the safety, tolerability, and PK characteristics of PSTB100 tablets.

Participants needed: 68
Trial details
Phase: Phase 1Age: 18-55Biological sex: AllType: InterventionalSponsor: Prospect Therapeutics (Nanjing) LimitedUpdated: Sep 4, 2026Locations: 1
Eligibility criteria

1.Healthy subjects aged 18-55 years (inclusive) at screening, with no gender res... [+5]

1.Females who are pregnant (positive or clinically abnormal pregnancy test resul... [+18]

Status: Recruiting

Effects of Hip Bump Manipulation Versus Sham Treatment in Healthy Adults

The purpose of this study is to objectively assess the effects of hip bump manipulation (HBM) on a healthy population aged 18-45 years. We hypothesize that the HBM will improve hip internal rotation passive range of motion, improve the strength of the hip external rotators, decrease compensatory motions in hip flexion during active range of motion, and improve bipodal landing mechanics. Human participants will be analyzed to determine whether the manipulation produces the intended clinical outcomes. While clinicians commonly use this technique, its effectiveness has yet to be substantiated through research. This technique is a high velocity low amplitude thrust to the greater trochanter which theorizes the quick stretch of the external rotator muscles and may improve a malpositioned femoral head within the acetabulum. These improvements may positively affect functional movements such as bipodal landing.

Participants needed: 60
Trial details
Age: 18-45Biological sex: AllType: InterventionalSponsor: Dominican University New YorkUpdated: Oct 14, 2025Locations: 1
Eligibility criteria

Healthy individuals [+1]

Diagnosed demoroacetabular labral tear [+7]

Status: Recruiting

Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of ID110521156 in Healthy Adult Subjects

The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics of multiple oral doses of ID110521156 in healthy adult subjects.

Participants needed: 36
Trial details
Phase: Phase 1Age: 19-50Biological sex: AllType: InterventionalSponsor: IlDong Pharmaceutical Co LtdUpdated: Dec 24, 2024Locations: 1
Eligibility criteria

Healthy subjects aged 19 to 50 years at the time of Screening. [+3]

Evidence or history of clinically significant hepatic, renal, neurological, immu... [+2]