Expanded Use PK of Dapivirine Vaginal Ring

NCT ID: NCT01952561

Last Updated: 2016-08-26

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 40 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2013-11-30
• Study Completion Date: 2014-05-31

Brief Summary

Study will evaluate the vaginal and blood pharmacokinetics of dapivirine from a vaginal ring containing 25 mg worn for 1, 2, 4, 8 or 12 months.

Conditions

Pharmacokinetics

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: NONE

Study Groups

2 weeks

Group Type: EXPERIMENTAL

dapivirine ring

Intervention Type: DRUG

1 week

Group Type: EXPERIMENTAL

dapivirine ring

Intervention Type: DRUG

4 weeks

Group Type: EXPERIMENTAL

dapivirine ring

Intervention Type: DRUG

8 weeks

Group Type: EXPERIMENTAL

dapivirine ring

Intervention Type: DRUG

12 weeks

Group Type: EXPERIMENTAL

dapivirine ring

Intervention Type: DRUG

Interventions

dapivirine ring

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Women 18 and ≤ 40 years of age who can give written informed consent

2. Available for all visits and consent to follow all procedures scheduled for the trial

3. Healthy, based on medical history, vital signs, physical examination, urinalysis, laboratory evaluations for genital infections, and laboratory evaluations for haematology and chemistry

4. HIV-negative as determined by an HIV test at the time of enrolment

5. On a stable form of contraception, defined as:

• A stable oral contraceptive regimen for at least 2 months prior to enrolment, OR
• Transdermal contraceptive patch for at least 3 months prior to enrolment, OR
• Long-acting progestins for at least 6 months prior to enrolment, OR
• An IUD inserted at least 3 months prior to enrolment, OR
• Have undergone surgical sterilisation at least 3 months prior to enrolment AND willing to use oral contraceptives if necessary to delay menstruation during the vaginal sampling period

6. Upon pelvic examination at the time of enrolment, the cervix and vagina appear normal as determined by the Investigator/Physician

7. Asymptomatic for genital infections at the time of enrolment

8. Willing to refrain from the use of topical vaginal medications, vaginal products or objects

9. Documentation of no abnormality on cervical cytology, including grossly bloody smear, within 90 days prior to screening

10. Willing to refrain from participation in any other research trial for the duration of this trial

11. Willing to provide adequate locator information for trial retention purposes and be reachable per local standard procedures, e.g. by home visit or telephone, or via family or close neighbour contacts

12. Willing to agree to abstain from all the following for a total of 2 days (48 hours) prior to each trial visit:

• Penile-vaginal intercourse
• Oral contact with her genitalia

13. Hepatitis B and C negative at the time of enrolment.

Exclusion Criteria

1. Currently pregnant or had their last pregnancy outcome within 3 months prior to screening

2. Currently breast-feeding

3. Currently or within two months of participation in any other clinical research trial involving investigational or marketed products prior to screening

4. Untreated symptomatic urogenital infections, e.g. urinary tract or other sexually transmitted infections, or other gynaecological conditions such as vaginal itching, pain, or discharge, within 2 weeks prior to enrolment

5. Have a Grade 2 or higher pelvic examination finding, according to the DAIDS Table for Grading the Severity of Adult and Pediatric Adverse Events;

6. History of significant urogenital or uterine prolapse, undiagnosed vaginal bleeding, urethral obstruction, incontinence or urge incontinence

7. Current vulvar or vaginal symptoms/abnormalities that could influence the trial results

8. Cervical cytology at screening that requires cryotherapy, biopsy, treatment (other than for infection), or further evaluation

9. Symptomatic genital herpes simplex virus (HSV) infection or a history of genital herpetic infection

10. Any Grade 2, 3 or 4 haematology, biochemistry or urinalysis laboratory abnormality at baseline (screening) according to the DAIDS Table for Grading the Severity of Adult and Pediatric Adverse Events;

11. Unexplained, abnormal bleeding per vagina during or following vaginal intercourse, or gynaecologic surgery within 90 days prior to enrolment

12. Any history of anaphylaxis or severe allergy resulting in angioedema; or a history of sensitivity/allergy to latex or silicone

13. Any serious acute, chronic or progressive or signs of cardiac disease, renal failure, or severe malnutrition

14. Have undergone a hysterectomy

15. Any condition(s) that, in the opinion of the Investigator, might interfere with adherence to trial requirements or evaluation of the trial objectives.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 40 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: Yes

Sponsors

International Partnership for Microbicides, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Other Identifiers

IPM 034

Identifier Type: -

Identifier Source: org_study_id