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Matrix Clinical Research | Los Angeles, CA

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A Study to Learn About the Study Medicine (Nirmatrelvir Plus Ritonavir) in Pregnant Women With COVID-19

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Pfizer

Status and phase

Enrolling
Phase 1

Conditions

COVID-19

Treatments

Drug: nirmatrelvir
Drug: ritonavir

Study type

Interventional

Funder types

Industry

Identifiers

NCT05386472
C4671035

Details and patient eligibility

About

The purpose of this clinical trial is to learn about how study medicine (Paxlovid, which contains nirmatrelvir and ritonavir) is changed and eliminated from the body, as well as its safety, and the extent to which side effects can be tolerated for treatment of pregnant women with mild or moderate COVID-19 compared to non-pregnant women with mild or moderate COVID-19.

This study is seeking participants who:

  • are expecting a healthy baby and are in their second or third trimester pregnancy and have mild or moderate COVID-19
  • are not pregnant and have mild or moderate COVID-19.

All participants in this study will take Paxlovid by mouth every 12 hours for 5 days. We will study the experiences of people receiving the study medicine. This will help us decide if the study medicine is safe.

All participants will take part in this study for at least 34 days; pregnant participants will take part until their delivery, so that the study duration may be up to 6 months, depending on their delivery date.

During this time, participants will have 7to 8 visits and, if pregnant, a visit at delivery. Around 2 to 3 visits and the delivery visit will be done in person (at the clinic or at the participant's home). The other 5 visits may be done over the phone, unless in-person visit is necessary as decided by the doctor. Blood samples will be collected on the first 4 to 5 study visits (and at other study visits, if necessary).

Enrollment

49 estimated patients

Sex

Female

Ages

18 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All cohorts: Mild-to-moderate COVID-19 infection confirmed in sample collected ≤5 days prior to enrollment; onset within 5 days prior to enrollment and presence of ≥1 sign/symptom on the day of enrollment.
  • Cohorts 1&2: Expecting single baby; Pregnant in 2nd trimester, 14 0/7 to 27 6/7 weeks of gestational age (Cohort 1) or 3rd trimester, ≥28 0/7 and ≤34 6/7 weeks of gestational age (Cohort 2), by ultrasound.
  • All cohorts: Otherwise healthy participants who are determined by medical history, physical examination, and clinical judgment to be appropriate for inclusion in the study

Exclusion criteria

  • All cohorts: Current need for hospitalization or anticipated need for hospitalization in the clinical opinion of the site investigator.
  • Cohorts 1&2: Prior/current major condition or illness of mother/fetus substantially increasing risk of study participation/completion or impacting pregnancy/fetal outcomes in investigator's judgement.
  • All cohorts: Current use of any medications that are highly dependent on CYP3A4 for clearance, and which are contraindicated in combination with nirmatrelvir/ritonavir.
  • All cohorts: Has received or is expected to receive monoclonal antibody treatment, convalescent COVID-19 plasma, or anti-viral treatment (eg, molnupiravir) for the current SARSCoV-2 infection.
  • All cohorts: Participants with moderate to severe kidney impairment

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

49 participants in 3 patient groups

Cohort 1
Experimental group
Description:
Pregnant women in their second trimester
Treatment:
Drug: ritonavir
Drug: nirmatrelvir
Cohort 2
Experimental group
Description:
Pregnant women in their third trimester
Treatment:
Drug: ritonavir
Drug: nirmatrelvir
Cohort 3
Experimental group
Description:
Non-pregnant women
Treatment:
Drug: ritonavir
Drug: nirmatrelvir

Trial contacts and locations

33

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Central trial contact

Pfizer CT.gov Call Center

Data sourced from clinicaltrials.gov

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