ClinicalTrials.Veeva

Menu

Safety and Pharmacokinetic Characteristics of DP-R206(Vitamin D3) in Healthy Adult Volunteers

A

Alvogen

Status and phase

Completed
Phase 1

Conditions

Healthy

Treatments

Drug: Vitamin D3
Drug: DP-R206

Study type

Interventional

Funder types

Industry

Identifiers

NCT01577849
DP-CTR206-02

Details and patient eligibility

About

The purpose of this study is to compare the pharmacokinetic characteristics of DP-R206 (150mg Ibandronate / 24,000 IU Vitamin D3 complex tablet, qd) and Vitamin D3 (24,000 IU Vitamin D3 , qd) after oral administration in healthy adult volunteers.

Full description

The number of patient is thirty-six. Patients were randomly assigned either a Vitamin D3 tablet(24,000 IU Vitamin D3, qd) first, DP-R206(150mg Ibandronate / 24,000 IU Vitamin D3 complex tablet, qd) Second or DP-R206(150mg Ibandronate / 24,000 IU Vitamin D3 complex tablet, qd) first, Vitamin D3 tablet(24,000 IU Vitamin D3 , qd) second.

Enrollment

36 patients

Sex

All

Ages

20 to 55 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 20 to 55 years of healthy volunteers

Exclusion criteria

  • Hypersensitivity Reaction about Ibandronate or other drugs(aspirin, antibiotics)

Trial design

36 participants in 2 patient groups

Vitamin D3
Active Comparator group
Treatment:
Drug: Vitamin D3
DP-R206
Experimental group
Treatment:
Drug: DP-R206

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems