Healthy Donors

5

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

Condition / disease
Location
Status: Recruiting

A Biospecimen Collection Study of Leukapheresis-Derived Circulating Tumor Cells, Immune Cells, and Progenitor Cells.

Primary Objective: This is a study to investigate the feasibility of harvesting, expanding, and selecting T lymphocytes from cancer patients and healthy volunteers. The preliminary objective of this study is aimed at selecting PD-1+ and CTLA4+ T cells and other cellular fractions from peripheral blood of cancer patients and healthy volunteers by using specific conjugated antibodies, evaluating their functional ex vivo anti-tumor cytotoxicity against targeted autologous tumor cells.

Participants needed: 1,500
Trial details
Age: 5+Biological sex: AllType: ObservationalSponsor: BioCytics, Inc.Updated: Mar 18, 2026Locations: 1
Eligibility criteria

Male or Female Adult ≥ 18 years of age. [+28]

Subjects with active infection requiring therapy (fever, localizing source) will... [+2]

Status: Not yet recruiting

Bioequivalence Study of Clonazepam 2 Mg Tablets

Demonstrate the bioequivalence in 1 study, in fasting condition of two formulations of clonazepam 2 mg Tablets / tablets immediate release in order to establish that there are no significant pharmacokinetic differences.

Participants needed: 24
Trial details
Phase: Phase 4Age: 18-50Biological sex: AllType: InterventionalSponsor: Centro de Atencion e Investigacion MedicaUpdated: Mar 10, 2025
Eligibility criteria

Women and men between 18 and 50 years of age at the time of signing the informed... [+12]

Subject with a diagnosis of renal, cardiac, hepatic, immunological, dermatologic... [+14]

Status: Recruiting

Novel Targets for the Development of Monoclonal Antibodies for Immunotherapy)

The first objective of the project consists in the preclinical validation of new possible molecular targets associated with intratumoral T regulatory cells. The second objective consists in the selection of monoclonal antibodies with therapeutic potential, specific for the selected targets.

Participants needed: 600
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Checkmab S.r.l.Updated: Feb 24, 2025Locations: 1
Eligibility criteria

blood donors [+2]

age below 18 years [+3]

Status: Not yet recruiting

Bioequivalence Study of Pentoxifylline 400 Mg in Healthy Subjects Under Fasting and Fed Conditions

Two bioequivalence studies of Pentoxifylline will be carried out in 40 healthy subjects, the first in a fasting condition 40 healthy subjects, the first in fasting condition and the second in postprandial condition. postprandial condition, the two studies follow the same design: Complete crossover design, randomized, comparative of two study formulations, in single dose of 400 mg of Pentoxifylline sustained release tablets, 2 periods, with a washout time of 7 days between doses, the 7 days between doses, participation as a subject in these studies involves a risk studies involves a higher than minimal risk for subjects.

Participants needed: 40
Trial details
Phase: Phase 4Age: 18-50Biological sex: AllType: InterventionalSponsor: Centro de Atencion e Investigacion MedicaUpdated: Feb 17, 2025
Eligibility criteria

Men or women between 18 and 50 years of age at the time of signing the informed... [+10]

Subject diagnosed with renal, cardiac, hepatic, immunologic, dermatologic, endoc... [+14]

Status: Recruiting

Investigating the Impact of the Seaweed Derived Food Additive, Carrageenan, on the Human Gut Microbiome

The goal of this study is to investigate whether a seaweed derived food additive, carrageenan, has an impact on the human gut microbiome in vivo. The primary purpose is to assess whether consumption of a carrageenan containing product for 4 weeks can alter the bacterial composition of the gut microbiome in healthy individuals and whether the addition of a prebiotic fibre, inulin, to the product has an enhanced beneficial impact of the gut composition. The main questions to answer are: Does the consumption of a confectionary item containing carrageenan and inulin lead to a positive impact on the faecal microbial community when compared to the confectionary item containing no carrageenan and no inulin (placebo)? Participants will be asked to consume 2 gummy sweets for 4 week period and provide stool and urine samples on 3 occasions over a 9 week period. Does the consumption of a confectionary item containing carrageenan and inulin improve gastrointestinal comfort measured using overall SHS-GI score when compared to baseline measurements recorded during run in period?

Participants needed: 99
Trial details
Age: 18-55Biological sex: AllType: InterventionalSponsor: University of ReadingUpdated: Dec 17, 2024Locations: 1
Eligibility criteria

Healthy individuals

Prescribed antibiotics in the last 3 months [+3]