Study of Ceftriaxone and Benzathine Penicillin G During Pregnancy (NCT07207876)
Phase IV Study of the Pharmacokinetics and Safety of Ceftriaxone and Benzathine Penicillin G During Pregnancy
🩺 Plain-English Summary (8th-Grade Level)
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.
Who can join: Review the eligibility criteria below.
Location: Site 5048, USC - Maternal Child Adolescent/Adult Center — Los Angeles, California
🧪 Interventions in This Study
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (9 Sites)
- Site 5048, USC - Maternal Child Adolescent/Adult Center — Los Angeles, California
- Site 5112, David Geffen School of Medicine at UCLA NICHD CRS — Los Angeles, California
- Site 5083, Rush Univ. Cook County Hosp. Chicago NICHD CRS — Chicago, Illinois
- Site 4001, Lurie Children's Hospital of Chicago (LCH) CRS — Chicago, Illinois
- Site 5040, SUNY Stony Brook NICHD CRS — Stony Brook, New York
- Site 5114, Bronx-Lebanon Hospital Center NICHD CRS — The Bronx, New York
- Site 5013, Jacobi Med. Ctr. Bronx NICHD CRS — The Bronx, New York
- Site 5128, Baylor College of Medicine/Texas Children's Hospital NICHD CRS — Houston, Texas
- Site 5129, IMPAACT/Gamma Project/UPR Pediatric HIV/AIDS Research CRS — San Juan,
📞 Contact the Study Coordinator
Phone: (202) 884-8480
Email: impaact.ctgov@fstrf.org
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
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Explore by condition: All Pregnancy clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.