Blood Levels of Tenofovir Gel in HIV Uninfected Pregnant Women Planning Cesarean Delivery

HIV Infections Clinical Trial

Official title:

Phase I Study of the Maternal Single-Dose Pharmacokinetics and Placental Transfer of Tenofovir 1% Vaginal Gel Among Healthy Term Gravidas

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00540605
• Other study ID #: MTN-002
• Secondary ID: 106001-U01-AI068
• Status: Completed
• Phase: Phase 1
• Est. completion date: January 2010

Study information

• Verified date: May 2012
• Source: National Institute of Allergy and Infectious Diseases (NIAID)
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

A new approach to HIV prevention currently being studied includes the use of topical microbicides, substances that kill microbes. The purpose of this study is to determine the levels of tenofovir, a microbicide in gel form, in HIV uninfected pregnant women who are expecting to deliver by cesarean.

Description:

There is an urgent need for HIV prevention methods that women can initiate and control themselves. Topical microbicides represent one such method. Tenofovir 1% vaginal gel was chosen as a high priority microbicide candidate due to its activity in target cells for HIV infection of the vagina and cervix and the low frequency of local and systemic toxicity observed in a prior HIV Prevention Trials Network (HPTN) trial utilizing tenofovir 1% gel. The purpose of this study is to assess term pregnancy single-dose pharmacokinetics (PK) of tenofovir 1% gel in HIV uninfected pregnant women.

The expected duration of participation for individually enrolled participants will depend on how early they enroll prior to the date of cesarean section, but may range from approximately 3 to 6 weeks. An initial screening/enrollment visit will occur approximately 1 to 4 weeks prior to the participant's scheduled cesarean section, but no more than 4 weeks before the delivery date. A targeted physical exam, medical and medication history assessment, blood and urine collection, and a pelvic exam will occur at screening/enrollment. Tenofovir gel will be administered vaginally approximately 2 hours before the expected time of cesarean section. On the day of gel administration and cesarean delivery, a targeted physical exam, medical and medication history assessment, a pelvic exam, maternal blood tenofovir level measurement, and collection of placental and endometrial tissues, cord blood, and amniotic fluid will occur.

After gel administration, PK measures will be taken at Hours 1, 2, 4, 6, 8, and 12; maternal blood tenofovir level measurement and a review of adverse events will also occur at these times. A 24-hour evaluation will occur between Hours 22 and 26. At this evaluation, a targeted physical exam, a review of adverse events, and tenofovir level measurement will occur. Each participant will be contacted between Days 10 and 18 to collect data on any adverse events they experience. In addition, an unscheduled visit may be necessary if an unresolved adverse event occurs on or after the 24-hour evaluation. If an unscheduled visit is required, the participant will undergo a targeted physical exam, medical and medication history assessment, blood and urine collection, a pelvic exam, and tenofovir level measurement.

Other known NCT identifiers

• NCT00572273

Recruitment information / eligibility

• Status: Completed
• Enrollment: 21
• Est. completion date: January 2010
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 18 Years to 45 Years

Eligibility

Inclusion Criteria:

• General good health

• HIV uninfected

• Hepatitis B surface antigen negative at screening and enrollment

• Viable, single pregnancy delivered by cesarean section planned between 37 0/7 to 41 6/7 weeks of pregnancy

• Normal Pap smear in the 12 months prior to study entry

• Willing to abstain from vaginal, anal, and receptive oral sex for at least 2 weeks after gel administration

• Willing to abstain from intravaginal products and practices (including douching) during study participation

Exclusion Criteria:

• Maternal or fetal condition that requires urgent cesarean section

• Documented rupture of the amniotic membranes

• Known disease in the mother that has a predictable negative effect on placental function

• Known placental/fetal abnormalities that could affect placental transfer. More information on this criterion can be found in the protocol.

• Previously demonstrated hypersensitivity to any components of tenofovir 1% gel

• Certain abnormal laboratory values

• Use of vaginal medications within 48 hours of study entry

• Untreated sexually transmitted infection (STI) or exposure to partner's STI, including chlamydia, gonorrhea, trichomoniasis, and nongonococcal urethritis

• Symptomatic vaginitis, including bacterial vaginosis and vulvovaginal candidiasis. Participants with asymptomatic signs of bacterial vaginosis and/or yeast not excluded.

• Participation in any other investigational drug or device trial within 30 days of study entry

• Any social or medical condition that, in the opinion of the investigator, would interfere with the study

Related Conditions & MeSH terms

• HIV Infections

Intervention

Drug:
• Tenofovir 1% vaginal gel
topical gel containing 1% tenofovir

Locations

Country	Name	City	State
United States	Pitt CRS	Pittsburgh	Pennsylvania

Sponsors (3)

Lead Sponsor	Collaborator
National Institute of Allergy and Infectious Diseases (NIAID)	Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), Microbicide Trials Network

Country where clinical trial is conducted

United States, 

References & Publications (2)

Carballo-Diéguez A, Balán IC, Morrow K, Rosen R, Mantell JE, Gai F, Hoffman S, Maslankowski L, El-Sadr W, Mayer K. Acceptability of tenofovir gel as a vaginal microbicide by US male participants in a Phase I clinical trial (HPTN 050). AIDS Care. 2007 Sep;19(8):1026-31. — View Citation

Mayer KH, Maslankowski LA, Gai F, El-Sadr WM, Justman J, Kwiecien A, Mâsse B, Eshleman SH, Hendrix C, Morrow K, Rooney JF, Soto-Torres L; HPTN 050 Protocol Team. Safety and tolerability of tenofovir vaginal gel in abstinent and sexually active HIV-infected and uninfected women. AIDS. 2006 Feb 28;20(4):543-51. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Maternal third trimester pharmacokinetic (PK) measures (AUC and Cmax)		Throughout study
Primary	Endometrial tenofovir levels		At Hours 1, 2, 4, 6, 8, 12, and 24 after drug administration
Primary	Placental transfer (cord blood tenofovir levels, placental tissue tenofovir levels, and amniotic fluid tenofovir levels)		At Hours 1, 2, 4, 6, 8, 12, and 24 after drug administration

External Links

•   Click here for the Microbicide Trials Network Web site
•   Haga clic aquí para ver información sobre este ensayo clínico en español.