Desmopressin Acetate 0.2 mg Tablets, Fasting

This study has been completed.
Sponsor:
Information provided by:
Teva Pharmaceuticals USA
ClinicalTrials.gov Identifier:
NCT00835211
First received: January 30, 2009
Last updated: September 1, 2009
Last verified: September 2009

January 30, 2009
September 1, 2009
July 2003
August 2003   (final data collection date for primary outcome measure)
  • Cmax - Maximum Observed Concentration [ Time Frame: Blood samples collected over 12 hour period ] [ Designated as safety issue: No ]
  • AUCinf - Area Under the Concentration-time Curve From Time Zero to Infinity (Extrapolated) [ Time Frame: Blood samples collected over 12 hour period ] [ Designated as safety issue: No ]
  • AUC0-t - Area Under the Concentration-time Curve From Time Zero to Time of Last Non-zero Concentration (Per Participant) [ Time Frame: Blood samples collected over 12 hour period ] [ Designated as safety issue: No ]
Bioequivalence based on Cmax and AUC [ Time Frame: 1 week ] [ Designated as safety issue: No ]
Complete list of historical versions of study NCT00835211 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
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Desmopressin Acetate 0.2 mg Tablets, Fasting
Comparative, Randomized, Single-Dose, 2-way Crossover Bioavailability Study of TEVA and Aventis Pharmaceuticals (DDAVP®) 0.2 mg Desmopressin Acetate Tablets in Healthy Adult Subjects Following a 0.8 mg Dose Under Fasting Conditions

The objective of this study was to compare the single-dose relative bioavailability of TEVA and Aventis Pharmaceuticals (DDAVP®) 0.2 mg desmopressin acetate tablets following a 0.8 mg dose under fasting conditions.

Criteria for Evaluation: FDA Bioequivalence Criteria

Statistical Methods: FDA bioequivalence statistical methods

Interventional
Phase 1
Allocation: Randomized
Endpoint Classification: Bio-equivalence Study
Intervention Model: Crossover Assignment
Masking: Open Label
Healthy
  • Drug: Desmopressin Acetate 0.2 mg Tablets
    4 x 0.2 mg, single-dose fasting
  • Drug: DDAVP® 0.2 mg Tablets
    4 x 0.2 mg, single-dose fasting
  • Experimental: 1
    Intervention: Drug: Desmopressin Acetate 0.2 mg Tablets
  • Active Comparator: 2
    Intervention: Drug: DDAVP® 0.2 mg Tablets
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
48
August 2003
August 2003   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Healthy adult non-smoker (for at least 3 months) or light smoking (less than 10 cigarettes per day for at least 3 months) male or female subjects, 18-55 years of age;
  • Weighing at least 60 kg for males and 52 kg for females;
  • Subjects who had a body mass index (BMI) less than 30;
  • Medically healthy subjects with clinically normal laboratory profiles and ECGs;

Females of childbearing potential should have either been sexually inactive (abstinent) for 14 days prior to the first dose and throughout the study or have been using one of the following acceptable birth control methods:

  • surgically sterile (tubal ligation, hysterectomy, bilateral oophorectomy) 6 months minimum. Proof was required for the hysterectomy and oophorectomy;
  • IUD in place for at least 3 months;
  • barrier methods (condom, diaphragm) with spermicide for at least 14 days prior to the first dose and throughout the study;
  • surgical sterilization of the partner (vasectomy for 6 months minimum);
  • hormonal contraceptives for at least 3 months prior to the first dose of the study.

Other birth control methods were deemed acceptable. Postmenopausal women with amenorrhea for at least 2 years were eligible.

  • Voluntarily consent to participate in the study.

Exclusion Criteria:

  • Female subjects who were pregnant or lactating.
  • Subjects who had been on a special diet (for whatever reason) during the 28 days prior to the first dose and throughout the study.
  • Any clinically significant illness within 4 weeks prior to dosing.
  • Subjects with any medical condition requiring regular treatment with prescription drugs.
  • The use of any pharmacological agents known to significantly induce or inhibit drug-metabolizing enzymes within 30 days prior to the first dose.
  • Subjects who, through completion of the study, would have donated in excess of: 500 mL of blood and/or plasma in 14 days; 1500 mL of blood and/or plasma in 180 days; 2500 mL of blood and/or plasma in 1 year.
  • Subjects who had donated plasma within 30 days prior to the first dose.
  • Subjects who ahd participated in another clinical trial within 30 days prior to the first dose.
  • Subjects who did not tolerate venipuncture.
  • History or presence of significant cardiovascular, pulmonary, hepatic, renal, hematologic, gastrointestinal, endocrine, immunologic, dermatologic, neurologic, or psychiatric disease.

In addition, the history or presence of:

  • hypersensitivity or idiosyncratic reaction to desmopressin or any other synthetic anti-diuretic hormones;
  • type IIB von Willebrand's disease;
  • personal or family bleeding disorder;
  • alcoholism or drug abuse within the past year.
Both
18 Years to 55 Years
Yes
Contact information is only displayed when the study is recruiting subjects
Canada
 
NCT00835211
AA04887
No
Not Provided
Teva Pharmaceuticals USA
Not Provided
Principal Investigator: Gaetano Morelli, M.D. MDS Pharma Services
Teva Pharmaceuticals USA
September 2009

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP