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ABT-072 · 1 trial · 1 indication
| Arm | Type | Description |
|---|---|---|
| 1 - Follow-up Study | OTHER | This is a follow-up study with no treatment and only samples being collected. |
| Name | Type | Description |
|---|---|---|
| ABT-072 | DRUG | Blood samples are being taken from subjects previously treated with ABT-072. |
Inclusion Criteria: \- Main Selection Criteria: A subject that has received either ABT-072 or placebo in a prior study involving ABT-072. Exclusion Criteria: \- The investigator considers the subject unsuitable for the study for any reasons inclusive of, but not limited to, failure to comply with...
ABT-072 is an investigational small molecule being developed for the treatment of Hepatitis C Virus (HCV) infection. It is a direct-acting antiviral agent studied in patients with chronic HCV infection. The drug is currently in clinical development and has not been approved by regulatory authorities.
ABT-072 is being developed by AbbVie Inc. (NYSE: ABBV), a global biopharmaceutical company. The drug is an investigational small molecule for the treatment of Hepatitis C Virus infection and is currently in Phase 2 clinical development.
ABT-072 is in Phase 2 clinical development for the treatment of Hepatitis C Virus infection. It is an investigational drug and has not received regulatory approval. The drug is being studied in a completed Phase 2 trial that assessed resistance to ABT-072 in HCV-infected subjects.
ABT-072 has been studied in one completed Phase 2 clinical trial, NCT00872196, which was a follow-up study to assess resistance to ABT-072 in HCV-infected subjects who had received the drug in prior studies. The trial enrolled 5 participants in the United States and was not randomized or double-blinded.
ABT-072 is a distinct investigational compound developed by AbbVie Inc. for Hepatitis C Virus infection. No alternative names for this drug have been reported. It is a small molecule antiviral agent that is being evaluated in clinical trials for its safety and efficacy.