Clinical TrialID 2578

A Phase I Dose Escalation Study of Synthetic Hypericin in HIV-Infected Patients With Less Than 300 CD4 Lymphocytes

NCT00000645

HIV Infections

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Record Fields

Scalar fields from the final clinical_trial record.

Clinical Trial Id
2578
Evidence Id
2578
Core Evidence Id
2578
Source Clinical Trial Id
2557
Herb2 Clinical Trial Id
HBCT002557
Nct Id
NCT00000645
Title
A Phase I Dose Escalation Study of Synthetic Hypericin in HIV-Infected Patients With Less Than 300 CD4 Lymphocytes
Status
Completed
Phase
Phase 1
Study Result
No
Study Condition
HIV Infections
Study Type
Interventional
Study Design
Allocation: |Intervention Model: |Masking: NONE|Primary Purpose: TREATMENT
Intervention
DRUG: Hypericin
Intervention Allocation
Intervention Model
Intervention Mask
Intervention Purpose
Treatment
Gender
All
Age
Adult, Older_Adult
Enrollment
32
Outcome Measure
Sponsor Collaborator
National Institute of Allergy and Infectious Diseases (NIAID)|VIMRx Pharmaceuticals
Funded By
NIH
Location
Beth Israel Deaconess - East Campus A0102 CRS, Boston, Massachusetts, 02215, United States|University of Minnesota, ACTU, Minneapolis, Minnesota, United States|NY Univ. HIV/AIDS CRS, New York, New York, 10016, United States
Other Id
ACTG 150|11125
Start Date
Primary Completion Date
Completion Date
1994-10
First Posted
2001-08-31
Results First Posted
Last Update Posted
2021-11-03
Study Document
Study Url
https://clinicaltrials.gov/study/NCT00000645
Title Cn
Title En
A Phase I Dose Escalation Study of Synthetic Hypericin in HIV-Infected Patients With Less Than 300 CD4 Lymphocytes
Bilingual Status
semi_complete