Status:
WITHDRAWN
A Study to Evaluate CSJ148 in Pregnant Women With Primary HCMV Infection
Lead Sponsor:
Novartis Pharmaceuticals
Conditions:
HCMV Infection
Eligibility:
FEMALE
18-65 years
Phase:
PHASE2
Brief Summary
The purpose of the study is to evaluate the feasibility of using CSJ148 to prevent congenital human cytomegalovirus (HCMV) in pregnant women with primary HCMV infection.
Detailed Description
This is a randomized, patient, investigator and sponsor blinded, placebo-controlled study in pregnant women with primary HCMV infection. The study has three periods: (I) screening (II) double-blinded ...
Eligibility Criteria
Inclusion
- Written informed consent must be obtained before any assessment is performed.
- Pregnant women ≥ 18 years of age with primary HCMV infection occurring between 6 and 24 weeks of gestation
- Ability to receive study drug within 6 weeks of the presumed onset of primary maternal infection.
- Able to communicate well with the investigator, to understand and comply with the requirements of the study.
Exclusion
- Confirmed or suspected fetal HCMV infection, defined as positive HCMV DNA in amniotic fluid or fetal ultrasound abnormalities suggestive of fetal HCMV disease.
- Prior treatment with any of the following within 30 days prior to enrollment: ganciclovir, valganciclovir, foscarnet, cidofovir, acyclovir (\>25 mg/kg/day IV), valacyclovir (\>3 gm/day oral), famciclovir (\>1500 mg/day oral), HCMV immune globulin, immune globulin (\>500 mg/kg), or any other medication with anti-HCMV activity.
- Any surgical or medical condition (other than pregnancy) which might increase the risk for thrombotic events if the patient is given immune-globulins. These conditions include cryoglobulinemia, monoclonal gammopathies, and hypertriglyceridemia (fasting level \>1000 mg/dL). The investigator should make this determination based on the patient's medical history and laboratory data.
- History of chronic hepatitis B, hepatitis C and human immunodeficiency virus (HIV) infection. Cured hepatitis C in not considered exclusionary.
- Patient request for medical interruption or termination of pregnancy before inclusion.
- Any surgical or medical condition which may jeopardize the patient or fetus in case of participation in the study. The investigator should make this determination in consideration of the patient's obstetrical history.
- Use of other investigational drugs at the time of enrollment, or within 5 half-lives of enrollment, or until the expected pharmacodynamic effect has returned to baseline, whichever is longer; or longer if required by local regulations.
- History of hypersensitivity to any of the study treatments or excipients or to drugs of similar chemical classes.
- Body weight \> 100 kilograms.
Key Trial Info
Start Date :
October 23 2018
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
November 15 2022
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT03369912
Start Date
October 23 2018
End Date
November 15 2022
Last Update
October 9 2018
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