← Back to Clinical Trials
Recruiting NCT05285735

NCT05285735 Observational Study of the Safety of Intravenous Artesunate Treatment of Pregnant Women and Their Infants

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT05285735
Status Recruiting
Phase
Sponsor Amivas Inc.
Condition Pregnancy
Study Type OBSERVATIONAL
Enrollment 25 participants
Start Date 2022-06-08
Primary Completion 2029-06-08

Eligibility & Interventions

Sex Female only
Min Age 15 Years
Max Age 100 Years
Study Type OBSERVATIONAL
All Conditions

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 25 participants in total. It began in 2022-06-08 with a primary completion date of 2029-06-08.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This study is a prospective observational study in which a female patient who received IV Artesunate while pregnant can volunteer to provide information about her pregnancy and the outcome of her pregnancy. Information will be collected from patient's provider, the patient's obstetrician, the child's pediatrician, or other relevant healthcare provider.

Eligibility Criteria

Inclusion Criteria: * Patient received IV Artesunate * Patient was pregnant while receiving IV Artesunate * Patient was at least 15 years of age * Patient or legal guardian/representative gave consent for the study and to collect data from her physicians Exclusion Criteria • None

Contact & Investigator

Central Contact

Katrina Riggs

✉ kriggs@fastttrackresearch.com

📞 3017622609

Principal Investigator

Bryan Smith, MD

PRINCIPAL INVESTIGATOR

Amivas Inc.

Frequently Asked Questions

Who can join the NCT05285735 clinical trial?

This trial is open to female participants only, aged 15 Years or older, up to 100 Years, studying Pregnancy. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT05285735 currently recruiting?

Yes, NCT05285735 is actively recruiting participants. Contact the research team at kriggs@fastttrackresearch.com for enrollment information.

Where is the NCT05285735 trial being conducted?

This trial is being conducted at Piscataway, United States.

Who is sponsoring the NCT05285735 clinical trial?

NCT05285735 is sponsored by Amivas Inc.. The principal investigator is Bryan Smith, MD at Amivas Inc.. The trial plans to enroll 25 participants.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology