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Recruiting No phase listed Observational

Study of Ceftriaxone and Benzathine Penicillin G During Pregnancy

ClinicalTrials.gov ID: NCT07207876

Public ClinicalTrials.gov record NCT07207876. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 5, 2026, 5:35 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Phase IV Study of the Pharmacokinetics and Safety of Ceftriaxone and Benzathine Penicillin G During Pregnancy

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

IMPAACT 2044 is a study to characterize the pharmacokinetics (PK) and safety of ceftriaxone and benzathine penicillin G during pregnancy. Up to 78 pregnant women receiving (1) ceftriaxone for indications other than syphilis or (2) benzathine penicillin G for treatment of syphilis from non-study clinical care providers will be enrolled at study sites located in the United States. Approximately 22 infants of pregnant participants receiving benzathine penicillin G will also be enrolled.

Study identification

NCT ID
NCT07207876
Recruitment status
Recruiting
Study type
Observational
Phase
Not listed
Enrollment
110 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
Not listed
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 15, 2026
Primary completion
Jan 14, 2027
Completion
Sep 29, 2027
Last update posted
Aug 5, 2026

2026 – 2027

United States locations

U.S. sites
8
U.S. states
4
U.S. cities
5
Facility City State ZIP Site status
Site 5048, USC - Maternal Child Adolescent/Adult Center Los Angeles California 90033 Recruiting
Site 5112, David Geffen School of Medicine at UCLA NICHD CRS Los Angeles California 90095 Recruiting
Site 5083, Rush Univ. Cook County Hosp. Chicago NICHD CRS Chicago Illinois 60612 Not yet recruiting
Site 4001, Lurie Children's Hospital of Chicago (LCH) CRS Chicago Illinois 60614 Recruiting
Site 5040, SUNY Stony Brook NICHD CRS Stony Brook New York 11794 Recruiting
Site 5114, Bronx-Lebanon Hospital Center NICHD CRS The Bronx New York 10457 Recruiting
Site 5013, Jacobi Med. Ctr. Bronx NICHD CRS The Bronx New York 10461 Recruiting
Site 5128, Baylor College of Medicine/Texas Children's Hospital NICHD CRS Houston Texas 77030 Recruiting

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07207876, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 5, 2026 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT07207876 live on ClinicalTrials.gov.

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