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Initiating daily oral PrEP during pregnancy

University of North Carolina, Chapel Hill · FDA-approved active Small molecule Quality 2/100

Initiating daily oral PrEP during pregnancy is a Small molecule drug developed by University of North Carolina, Chapel Hill. It is currently FDA-approved. Also known as: Tenofovir disoproxil fumarate (TDF)/emtricitabine (FTC) or lamivudine (3TC) (FTC/TDF or TDF/3TC).

At a glance

Generic nameInitiating daily oral PrEP during pregnancy
Also known asTenofovir disoproxil fumarate (TDF)/emtricitabine (FTC) or lamivudine (3TC) (FTC/TDF or TDF/3TC)
SponsorUniversity of North Carolina, Chapel Hill
ModalitySmall molecule
PhaseFDA-approved

Approved indications

No approved indications tracked.

Common side effects

No common side effects on file.

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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Frequently asked questions about Initiating daily oral PrEP during pregnancy

What is Initiating daily oral PrEP during pregnancy?

Initiating daily oral PrEP during pregnancy is a Small molecule drug developed by University of North Carolina, Chapel Hill.

Who makes Initiating daily oral PrEP during pregnancy?

Initiating daily oral PrEP during pregnancy is developed and marketed by University of North Carolina, Chapel Hill (see full University of North Carolina, Chapel Hill pipeline at /company/university-of-north-carolina-chapel-hill).

Is Initiating daily oral PrEP during pregnancy also known as anything else?

Initiating daily oral PrEP during pregnancy is also known as Tenofovir disoproxil fumarate (TDF)/emtricitabine (FTC) or lamivudine (3TC) (FTC/TDF or TDF/3TC).

What development phase is Initiating daily oral PrEP during pregnancy in?

Initiating daily oral PrEP during pregnancy is FDA-approved (marketed).

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