Skip to content

Drug-drug interaction in the co-administration of the antiretroviral drugs and the antischistomicide praziquantel

Drug-drug interaction in the co-administration of the antiretroviral drugs and the antischistomicide praziquantel

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
PACTR
Registry ID
PACTR202102566734864
Enrollment
32
Registered
2021-02-03
Start date
2019-05-13
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HIV/AIDS schistosomiasis

Interventions

Praziquantel
Efavirena
Ritonavir

Sponsors

AiBST
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: Male Black Zimbabwean Age between 18 and 40 years BMI between 18 and 30 HIV, Hepatitis B and C negative Able to give consent Non-smoking Lab screening and ECG within the limits stipulated in the protocol Healthy as determined by medical examination

Exclusion criteria

Exclusion criteria: HIV positive any current or past history of psychiatric disorder subjects receiving any prescription or over the counter product use of any recreational drug subjects who have eaten grapefruit or drunk grapefruit juice during the last 15 days before administration of study drug subjects who had xanthine containing beverages (coffee, tea, chocolates, etc) 48 hours prior to study drug administration history of hepatic, renal, GI, heart, lung, neurological, endocrine, chronic infections or disease subjects suffering from any acute disease at screening or check in Alanine S. Transaminase (AST)/ Alanine L. Transaminase (ALT) >3 times upper limit of normal (ULN) Bilirubin >2.5 times ILN Amylase > 2 times ULN Absolute Neutrophil Count 50 000 cells/mm3 serum creatinine >2.5 mg/dl

Design outcomes

Primary

MeasureTime frame
AUC, Cmax

Secondary

MeasureTime frame
Tmax, half life and elimination rate constant

Countries

Zimbabwe

Contacts

Public ContactGeorginah Nyabadza

Clinical Trial Manager

georginah.nyabadza@aibst.com+263773069254

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Aug 9, 2026