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Evaluation of safety, tolerability and sensory evaluation of HEFD-072006 in Healthy Adults

Safety, Tolerability and Sensory evaluation of HEFD-072006 in Healthy Adult Volunteers - An Open-Label, Single-Arm Clinical Study

Status
Active, not recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/01/048929
Enrollment
12
Registered
2023-01-11
Start date
Unknown
Completion date
Unknown
Last updated
2023-02-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

None listed

Sponsors

Himalaya Wellness Company
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Healthy adult subjects of either sex aged between >= 18 to 2. Subjects willing to sign informed consent and follow the study procedure. 3. Has not participated in a similar investigation in the past four weeks. 4. Subjects willing to refrain taking any other similar supplements during the study period.

Exclusion criteria

Exclusion criteria: 1. Subjects with clinically significant serious cardiovascular, cerebrovascular, respiratory, hepatic, renal disease, congenital or any other disorder. 2. Subject with abnormal lab values detected at the time of screening shall be excluded. 3. A known history or present condition of allergic response to pharmaceutical products its components or ingredients in the investigational product. 4. Pre-existing systemic disease necessitating long-term medications. 5. Genetic and endocrinal disorders. 6. Subjects who refused to sign informed consent. 7. Pregnant and lactating women.

Design outcomes

Primary

MeasureTime frame
Incidence of any adverse or serious adverse events reported or observed during the study periodTimepoint: 7 days

Secondary

MeasureTime frame
Overall compliance of the subject to the study medicationTimepoint: 7 days

Countries

India

Contacts

Public ContactKavitha R

Himalaya Wellness Company

dr.sooryanarayan.h@himalayawellness.com08067549919

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026