Multicenter study to assess the safety of HRF-10071 in newly diagnosed HIV infected patient.
- Conditions
- Health Condition 1: B20- Human immunodeficiency virus [HIV]disease
- Registration Number
- CTRI/2022/12/048577
- Lead Sponsor
- Hetero Labs Limited
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Closed to Recruitment of Participants
- Sex
- Not specified
- Target Recruitment
- 0
1. Patients willing to give audio & written, signed, and dated informed consent to participate in the study.
2. Treatment-naive: No prior intake/ administration of anti-retrovirals (in combination or monotherapy) received after the diagnosis of HIV-1 infection or HBV infection
3. Documented HIV infection and Screening plasma HIV-1 RNA >=5000 copies/milliliter (mL).
4. Cluster Designation 4 Positive (CD4+) T cell count >=350 cell/mm3 at screening
5. Body weight >=50.0 kilograms (kg) for men and >=45.0 kg for women and body mass index (BMI) within the range 18.5-31.0 kg/meter square (kg/m2) (inclusive)
6. Subjects who are healthy (other than HIV infection) and immunocompetent as determined by the Investigator or medically qualified designee based on a medical evaluation including medical history, laboratory tests, and cardiac monitoring.
7. Females of childbearing potential who are sexually active must agree to use barrier contraception and can neither be pregnant nor lactating from screening throughout the duration of the study. The serum pregnancy test at screening and urine pregnancy test before dosing on day 01 must be negative for female patients of childbearing potential. Male partners of female patients and male patients should agree to use barrier contraception throughout the study period
1. History of sensitivity to any of the study medications, or components thereof or a history of drug or other allergy that, in the opinion of the investigator or Medical Monitor, contraindicates their participation.
2. Patients with the Hepatitis B surface antigen (HBsAg) and Hepatitis C antibody positive at screening or with 3 months prior to screening.
3. Patients with known brain metastasis.
4. History of ongoing or clinically relevant hepatitis within the previous 6 months.
5. Hemoglobin <10.0 g/dL; Absolute neutrophil count <1000 cells/mm3; platelet count <=100,000 cells/mm3
6. Alanine aminotransferase (ALT) >=1.5 times upper limit of normal (ULN); Aspartate aminotransferase (AST) >=1.5 times ULN; Alkaline phosphatase >=1.5 times ULN; bilirubin >ULN.
7. Patients with primary HIV infection, evidenced by acute retroviral syndrome (e.g., fever, malaise, fatigue, etc) and/or evidence of recent (within 3 months) documented viremia without antibody production and/or evidence of recent (within 3 months) documented seroconversion.
8. Any history or evidence of viral resistance based on the presence of any major resistance associated mutation (International acquired immunodeficiency syndrome [AIDS] society).
9. Any history or evidence (prior to study screening period) of the presence of resistance-associated mutations on Gag gene.
10. Creatinine Clearance less than 50 mL/minute.
11. Active Treatment for a viral infection other than HIV-1, such as Hepatitis B, with an agent that is active against HIV-1
12. Treatment with an HIV-1 immunotherapeutic agent within 90 days of Screening
13. Unstable liver disease - as defined by any of the following- presence of ascites, encephalopathy, coagulopathy, hypoalbuminemia, esophageal or gastric varices, or persistent jaundice or cirrhosis, known biliary abnormalities -with the exception of Gilbert syndrome or asymptomatic gallstones or otherwise stable chronic liver disease per investigator assessment.
14. Presence of moderate-to-severe hepatic impairment (Class B or C) as determined by Child-Pugh classification.
15. A pre-existing condition interfering with normal gastrointestinal anatomy or motility (e.g., gastroesophageal reflux disease [GERD], gastric ulcers, gastritis), hepatic and/or renal function, that could interfere with the absorption, metabolism, and/or excretion of the study drugs or render the patient unable to take oral study treatment.
16. Any acute laboratory abnormality at screening which, in the opinion of the investigator, should preclude participation in the study of an investigational compound.
17. Any Grade 2-4 laboratory abnormality at screening, with the exception of creatine phosphokinase (CPK) and lipid abnormalities (e.g., total cholesterol, triglycerides, etc), ALT, AST and ALP (described above)
18. Any history of significant underlying psychiatric disorder, including but not limited to schizophrenia, bipolar disorder with or without psychotic symptoms, other psychotic disorders, or schizotypal (personality) disorder.
19. Any history of major depressive disorder with or without suicidal features, or anxiety disorders, that required medical intervention (pharmacologic or not) such as hospitalization or other inpatient treatment and/or chronic (more than 6 months) outpatient treatment.
20. Any pre-existing physical or other psychiatric co
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method