Bioequivalence Study of Paricalcitol Capsules, 4 mcg Under Fasting Conditions

NCT02322632 | Completed Phase 1 DMC

• 1 other identifier: 280-01
• Study Type: interventional
• Target: 69
• Locations: 1 country
• Sites: 1

Brief Summary

An open-label, balanced, randomized, two-treatment, two-sequence, two-period, single-dose, crossover oral bioequivalence study in healthy subjects under fasting conditions.

Conditions

Healthy

Outcome Measures

Primary Outcomes (1)

• Area under curve

  0.25, 0.5, 0.75, 1.0, 1.25, 1.5, 1.75, 2.0, 2.5, 3.0, 3.5, 4.0, 6.0, 8.0, 10.0, 12.0, 16.0, 24.0, 36.0, 48.0 and 60.0 hours post-dose

Study Arms (2)

Paricalcitol Capsules, 4 mcg

EXPERIMENTAL

Paricalcitol Capsules, 4 mcg of Dr. Reddy's Laboratories Limited

Drug: Paricalcitol Capsules, 4 mcg

Zemplar Capsules, 4 mcg

EXPERIMENTAL

Zemplar Capsules, 4 mcg of Abott Laboratories USA

Drug: Paricalcitol Capsules, 4 mcg

Interventions

Paricalcitol Capsules, 4 mcg DRUG

Paricalcitol Capsules, 4 mcg of Dr. Reddy's Laboratories Limited

Also known as: Zemplar

Paricalcitol Capsules, 4 mcg; Zemplar Capsules, 4 mcg

Eligibility Criteria

• Age: 18 Years - 55 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Healthy, adult, human volunteers between 18 and 55 years of age (both inclusive) living in and around Ahmedabad city of western part of India.
• Having a Body Mass Index (BMI) between 18.5 and 24.9 (both inclusive), calculated as weight in kg/height in m2.
• Have no significant diseases or clinically significant abnormal findings during screening, medical history, clinical examination, laboratory evaluations, 12- lead ECG and X-ray chest (postero-anterior view) recordings.
• Volunteers who have normal calcium, phosphorous status and no hypertensive status in order to avoid effect on vitamin D concentration in blood.
• Able to comply with the study procedures, in the opinion of the Principal investigator.
• Able to give voluntary informed consent for participation in the trial.
• In case of female subjects\*:
• Surgically sterilized at least 6 months prior to study participation; Or
• If of child bearing potential is willing to use a suitable and effective double barrier contraceptive method or intra uterine device during the study.
• Urine pregnancy test (for female subjects\*) must be negative at the time of screening. \*No female subjects were enrolled in the study.

You may not qualify if:

• Known hypersensitivity or idiosyncratic reaction to Paricalcitol or to any of its excipients or any drug or any substance.
• History or presence of any disease or condition which might compromise the haemopoietic, renal, hepatic, endocrine, pulmonary, central nervous, cardiovascular, immunological, dermatological, gastrointestinal or any other body system.
• Ingestion or Use of any medication at any time in 14 days prior to dosing. In any such case subject selection will be at the discretion of the Principal Investigator.
• Any history or presence of asthma (including aspirin induced asthma) or nasal polyp or NSAID induced urticaria.
• Consumption of Grapefruits or its products within a period of 48 hours prior to check-in.
• A recent history of harmful use of alcohol(less than 2 years), i.e. alcohol consumption of more than 14 standard drinks per week for men and more than 7 standard drinks per week for women (A standard drink is defined as 360 ml of beer or 150 ml of wine or 45 ml of 40% distilled spirits, such as rum, whisky, brandy etc). " or consumption of alcohol or alcoholic products within 48 hous prior to check-in.
• Smokers, who smoke 10 or more than 10 cigarettes / day or inability to abstain from smoking during the study.
• The presence of clinically significant abnormal laboratory values during screening.
• Use of any recreational drugs or history of drug addiction or testing positive in pre-study drug scans.
• History or presence of psychiatric disorders.
• A history of difficulty with donating blood.
• A positive hepatitis screen including hepatitis B surface antigen and anti- HCV antibodies.
• A positive test result for anti-HIV antibody.
• An unusual diet, for whatever reason (e.g. low-sodium), for four weeks prior to receiving the study drug and throughout the subjects' participation in the study. In any such case subject selection will be at the discretion of the Principal Investigator. Nursing mothers (females)\*. \*No female subjects were enrolled in the study.

Sponsors & Collaborators

• Dr. Reddy's Laboratories Limited: lead

Study Sites (1)

Lambda Therapeutic Research Ltd

Ahmedabad, Gujarat, 3 80 061, India

Location

MeSH Terms

Interventions

paricalcitol

Study Officials

• Dr. Pankaj Kumar Jha, MD

  Lambda Therapeutic Research Limited

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: CROSSOVER
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: December 18, 2014
• First Posted: December 23, 2014
• Study Start: November 1, 2010
• Primary Completion: December 1, 2010
• Study Completion: February 1, 2011
• Last Updated: December 23, 2014

Record last verified: 2014-12

Locations

IN (1)