Pharmacokinetics of Sofosbuvir/Daclatasvir in HCV-infected Lactating Women

NCT ID: NCT04852614

Last Updated: 2022-08-23

Basic Information

• Recruitment Status: UNKNOWN
• Total Enrollment: 10 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2020-12-01
• Study Completion Date: 2023-12-01

Brief Summary

This is a prospective, observational, open-label, pharmacokinetic study will evaluate PK of SOF/DAC in lactating HCV-infected females at weaning or women who voluntarily decided to forego breastfeeding to initiate HCV infection treatment. Therefore, drug concentrations can be determined in maternal plasma and milk without risk to the children. HCV infected women at weaning after various durations of breastfeeding and HCV infected women who wish to initiate treatment immediately after delivery and forego breastfeeding will be recruited to start treatment under the guidance of their physician with SOF/DAC to determine M/P ratios of each of SOF, GS-331007 and DAC.

Detailed Description

Eligible women will be advised to arrange for initiation of treatment with their physician once they decide to stop breastfeeding. Treatment will be initiated once the women decide to wean their children and a warning will be given to abstain from any breast-feeding once treatment is started. This treatment is prescribed by the physician either the patients choose to participate in the study or not. In addition, effective contraceptive methods should be used. The treatment consists of SOF/DAC: 400 mg sofosbuvir and 60 mg daclatasvir administered with food for 12 weeks.

All recruited patients will be screened for the following data at baseline: Serum creatinine, bilirubin, albumin, AST, ALT, prothrombin time (PT), CBC, and viral load by PCR. The patient's general and demographic information (age, gender, height, and weight), comorbidities, and concurrent medications will be assessed and recorded in a specially designed patient data sheet.

The study will be conducted in the Faculty of Medicine Ain-Shams Research Institute Clinical Research Center (MASRI -CRC). After the first dose, women will be instructed to express their milk and discard it on the first two days and come to the research center on the third day for plasma and milk sampling. Patients will be instructed to take the dose on time especially the day before sampling. They will be asked to record the time of dose administration. They might be also followed up by telephone calls

Conditions

Hepatitis C Virus Infection

Study Design

• Observational Model Type: CASE_ONLY
• Study Time Perspective: PROSPECTIVE

Interventions

Pharmacokinetic test

Blood samples will be collected 48 hours after the first dose on day 3 of the observed intake of the study medication at the following time points: t=0 (pre-dose), 1, 2, 3, 4, 8 and 12 hours post ingestion (7 samples) (3 mL each), Breast milk samples will be collected by emptying both breasts at 0, 2, 4, 8 and 12 hours (5 samples).

Intervention Type: DIAGNOSTIC_TEST

Eligibility Criteria

Inclusion Criteria

• Patient is at least 18 years of age at the day of screening.
• Confirmed HCV infection by PCR and known genotype (GT) 1, 4, 5, or 6.
• Female lactating patient, who will wean their children on starting treatment and ensure not to breastfeed after start treatment.
• Patients with an indication for SOF/DAC treatment for the treatment of chronic HCV.
• Patient is able and willing to sign the Informed Consent Form.
• Patient is able and willing to follow protocol requirements.

Exclusion Criteria

• Need for co-treatment with ribavirin.
• HepBSAg positive test at screening.
• Treatment with rosuvastatin.
• Medicinal products that are potent P-glycoprotein (P-gp) and or CYP3A4 inducers in the intestine (rifampicin, rifabutin, St. John's wort [Hypericum perforatum], carbamazepine, phenobarbital and phenytoin).
• HIV co-infected patients using antiretroviral agents possibly interacting with SOF/DAC.
• Drugs associated with bradycardia including amiodarone.
• History of heart block.
• eGFR < 30 ml/min/1.73 m2.
• Compensated cirrhosis, based on historical data, evidence of decompensated cirrhosis by ascites, encephalopathy, or variceal hemorrhage and/or abnormal ALT/AST/INR/thrombocytes indicating cirrhosis.
• Relevant history or current condition that might interfere with drug absorption, distribution, metabolism or excretion except for conditions related to HCV.
• Clinically relevant low hemoglobin concentration at screening.
• Pregnancy
• Refusal to use proper contraception during treatment

• Minimum Eligible Age: 18 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

Ain Shams University

OTHER

Sponsor Role: lead

Responsible Party

Manal Hamdy El-Sayed

Director of Faculty of Medicine Ain Shams University Research Institute

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Manal SE El-Sayed, M.D

Role: PRINCIPAL_INVESTIGATOR

Ain Shams University, Faculty of Medicine

Locations

Faculty of Medicine Ain Shams University Research Institute- Clinical Research Center

Cairo, Non-US, Egypt

Site Status: RECRUITING

Countries

Egypt

Central Contacts

Manal H El-Sayed, MD

Role: CONTACT

manalhelsayed@yahoo.co.uk

01227461120 ext. 002

Fatma Soliman E Ebeid, MD

Role: CONTACT

dr.fatma_ebeid@yahoo.com

01095569596

Facility Contacts

Fatma Soliman E Ebeid

Role: primary

dr.fatma_ebeid@yahoo.com

01095569596

Other Identifiers

CL 2489

Identifier Type: -

Identifier Source: org_study_id