Single Dose Bioequivalence Study of Darifenacin Tablets 7.5 mg in Fed Healthy Volunteers.

Bioequivalency Clinical Trial

Official title:

Comparative Bioavailability of Darifenacin Extended Release Oral Formulation [Darisec(R)7.5 mg vs. Enablex(R)7.5 mg]: Single-dose, Postprandial State, Randomized, Two-sequence, Two-period, Crossover Study in Healthy Volunteers.

Clinical Trial Details — Status: Unknown status

Administrative data

• NCT number: NCT01229280
• Other study ID #: BDBEQ_DFNLP/ELEA_010
• Status: Unknown status
• Phase: Phase 1
• First received: October 26, 2010
• Last updated: October 26, 2010
• Start date: December 2010
• Est. completion date: February 2011

Study information

• Verified date: October 2010
• Source: Center for Clinical Pharmacology Research Bdbeq S.A.
• Contact: Federico Santoro, MD
• Phone: +541143794300
• Email: santorof[@]elea.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The proposed study was designed as a randomized two-sequence, two period crossover trial to assess the bioequivalence, pharmacokinetic profiling and safety of a brand generic formulation of darifenacin [Darisec(R) 7.5 mg] vs. the innovator [Enablex(R)7.5 mg]in healthy volunteers in postprandial state.

Description:

Darifenacin is a muscarinic receptor antagonist drug used to treat overactive bladder. There is a new formulation of darifenacin extended release developed by an argentinian pharmaceutical company. A bioequivalence study will be performed to validate pharmaceutical development before introducing the product in the market.

The purpose in this study is to evaluate the relative bioavailability, pharmacokinetic profiling and safety of a brand generic formulation of darifenacin [Darisec(R) 7.5 mg] vs. the innovator [Enablex(R) 7.5 mg]in 24 healthy uruguayan volunteers after a high fat breakfast of 1000 calories (50% fat, 35% carbohydrates, and 15% proteins)to establish their average bioequivalence.

The bioequivalence will be evaluated using:

• The Area Under the Curve (AUC),

• The peak plasma concentration (Cmax).

The pharmacokinetic characteristics of the drug formulations will be described calculating:

• The time to peak concentration (Tmax)

• The elimination constant (Ke)

• The elimination half-life (t1/2e)

• The systemic clearance (Cls)

Safety will be evaluated recording:

• Reported adverse events

• Vital signs (blood pressure, heart rate, body temperature)

• Laboratory analysis (hemogram, hepatic enzymes, creatinine, sugar in blood, etc.)

• EKG and chest XRays

Bioequivalence will be claimed if the drugs comply with local and FDA regulatory requirements:

• Mean AUCt/AUCr and 90% confidence interval within 0.80-1.25

• Mean Cmaxt/Cmaxr and 90% confidence interval within 0.80-1.25

Pharmacokinetic profiling will be evaluated by describing the pharmacokinetic characteristics of both drug in adequate two-way tables.

Safety will be evaluated comparing incidence of adverse events/adverse effects for both products.

Recruitment information / eligibility

• Status: Unknown status
• Enrollment: 24
• Est. completion date: February 2011
• Est. primary completion date: January 2011
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 50 Years

Eligibility

Inclusion Criteria:

• Healthy male or female subjects 18 to 50 years of age (inclusive).

• In good health, as determined by lack of clinically significant abnormalities at screening as judged by the physician.

• Female subjects are required to use a medically accepted method of hormonal contraception or abstinence throughout the entire study period and for one week after the study is completed.

• Body mass index within the range of 18.5 and 29.9 kg/m2 and weight at least 45 kg.

Exclusion Criteria:

• Known hypersensitivity or severe adverse event to darifenacin or similar drugs.

• Urinary, retention, narrow-angle glaucoma, myasthenia gravis, severe hepatic impairment, severe ulcerative colitis, toxic megacolon.

• Symptomatic hiatus hernia, erosive or symptomatic gastroesophageal reflux disease/heartburn (>2 days in a week), severe constipation, gastrointestinal obstructive disorder, and gastric retention.

• Clinically significant cardiac abnormalities, fainting, low blood pressure upon standing, irregular heartbeats.

• Acute or chronic bronchospastic disease(including asthma and Chronic Obstructive Pulmonary Disease).

• Clinically significant drug allergy or history of atopic allergy (asthma, urticaria, eczematous dermatitis).

• Smokers of more than 5 cigarettes a week.

• Regular use of any drug known to induce or inhibit hepatic drug metabolism (particularly those that affect CYP2D6) within 30 days prior to each study drug administration.

• Any surgical or medical condition which might significantly alter the absorption, distribution, metabolism, or excretion of drugs which may jeopardize participation in the study.

• Immunodeficiency diseases, including a positive HIV (Elisa or Western blot) test result.

• Positive Hepatitis B Surface antigen (HBsAg) or Hepatitis C results.

• Drug or alcohol abuse within the 6 months prior to dosing.

• Use of prescription drugs within 1 month prior to dosing, or over-the-counter medication (vitamins, herbal supplements, dietary supplements)within 2 weeks prior to dosing. Paracetamol and ibuprofen are acceptable.

• Participation in any clinical investigation within 12 weeks prior to dosing.

• Donation or loss of 400 ml or more of blood within 8 weeks prior to dosing.

• Significant illness within 2 weeks prior to dosing.

• Other protocol-defined inclusion/exclusion criteria may apply.

Related Conditions & MeSH terms

• Bioequivalency

Intervention

Drug:
• Darifenacin
Single dose 7.5 mg tablets of darifenacin
• Darifenacin
Single dose 7.5 mg tablets of Darifenacin

Locations

Country	Name	City	State
Uruguay	Center for Clinical Pharmacology Research (CCPR) Bdbeq S.A. Hospital Italiano.	Montevideo

Sponsors (2)

Lead Sponsor	Collaborator
Center for Clinical Pharmacology Research Bdbeq S.A.	Laboratorio Elea S.A.C.I.F. y A.

Country where clinical trial is conducted

Uruguay, 

References & Publications (5)

Croom KF, Keating GM. Darifenacin: in the treatment of overactive bladder. Drugs Aging. 2004;21(13):885-92; discussion 893-4. Review. — View Citation

Dmochowski RR, Appell RA. Advancements in pharmacologic management of the overactive bladder. Urology. 2000 Dec 4;56(6 Suppl 1):41-9. Review. — View Citation

Kerbusch T, Wählby U, Milligan PA, Karlsson MO. Population pharmacokinetic modelling of darifenacin and its hydroxylated metabolite using pooled data, incorporating saturable first-pass metabolism, CYP2D6 genotype and formulation-dependent bioavailability. Br J Clin Pharmacol. 2003 Dec;56(6):639-52. — View Citation

Skerjanec A. The clinical pharmacokinetics of darifenacin. Clin Pharmacokinet. 2006;45(4):325-50. Review. — View Citation

Staskin DR. Overactive bladder in the elderly: a guide to pharmacological management. Drugs Aging. 2005;22(12):1013-28. Review. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Extent of absorption	Extent of absorption will be measured using the area under the plasma concentration of darifenacin vs time from time 0 to the last sample point (AUC0-t) and from time 0 to infinity (AUC0-inf.	72 hours
Primary	Rate of absorption	Rate of abosorption will be measured using peak concentration of darifenacin (Cmax)taken from the concentration vs. time curve.	72
Secondary	Time to peak concentration (tmax)	Tmax is the time elapsed from ingestion of darifenacin tablets to plasma peak concentration (Cmax)	72
Secondary	Elimination rate constant (Ke)	The elimination rate constant is the fractional rate of drug disappearance form the peripheral compartement, measured in the log-linear elimination phase.	72 hours
Secondary	Elimination Half-life (t1/2e)	t1/2e is the time in which the concentration in the log-linear elimination phase drops by half.	72 hours
Secondary	Systemic clearance (Cls)	Cls is the amount of plasma volume units that are totally cleared of the drug in the unit of time.	72 hours