A randomized, double blind, balanced, single center, two treatment, two period, two sequence, single dose, crossover relative bioavailability study of turmeric extracts in healthy human adult subjects, under fasting conditions.

Exodus Research Acer0 sites16 target enrollmentTBD

Overview

No summary available.

Registry

who.int

Start Date

TBD

End Date

TBD

Last Updated

4 years ago

Study Type

Ba/be

Sponsor

Exodus Research Acer

•a.Be healthy male or non\-pregnant and non\-lactating female 18 to 45 years of age, both ages inclusive.
•b.Be healthy male or non\-pregnant and non\-lactating female of BMI within 18\.50 to 24\.99 Kg/ m2\. Volunteers weighing less than 50 kg will not be enrolled.
•c.Be able to communicate effectively with the study personnel.
•d.Be a non consumer (user) of tobacco (not consumed tobacco in the past 6 months) or a mild or moderate consumer (user) of tobacco.
•e.Have no evidence of underlying disease during screening medical history and whose physical examination is performed within 21 days prior to check in of period one.
•f.Be medically healthy with clinically acceptable laboratory profiles, ECG (performed within 21 days prior to check\-in of period one) and chest X\-ray (performed within 6 months prior to check\-in of period one).
•g.Have given the written informed consent for voluntary participation in the study.
•h.Be declared eligible to participate in the study by the investigator(s).
•i.In addition, female volunteers selected for the study must:
•i)Be using a medically acceptable form of birth control (such as foams, jellies, diaphragm, intra\-uterine device (IUD) or abstinence) for the duration of the study as judged by the investigator(s) Or

•a.Participation in any bioavailability, bioequivalence, Pharmacokinetic study or received an investigational drug within a period of 3 months prior to check in of period one.
•b.History of drug abuse, or alcohol dependence or abuse.
•c.History of any allergies (asthma, urticaria) including drug allergies.
•d.Known hypersensitivity or allergy to curcuminoids or any of the excipients or related drugs
•e.Severe consumer of tobacco.
•f.Presence of a clinically significant disorder involving the cardiovascular,respiratory, renal, gastrointestinal, hepatic, immunologic, hematological, endocrine, or nervous system or psychiatric disease or other conditions that may interfere with the absorption, distribution, metabolism or excretion of study drug, or would place the subject at increased risk, as determined by the investigator.
•g.Volunteers who have,
•i.Systolic blood pressure less than 90 mm of Hg or more than 140 mm of Hg. Diastolic blood pressure less than 60 mm of Hg or more than 90 mm of Hg. Minor deviations 2\-4 mm of Hg at check\-in may be acceptable at the discretion of the physician /investigator.
•ii.Pulse rate below 60 per minute or above 100 per minute.
•iii.Respiratory rate below 15 or above 20 breaths per minute.

Not specified