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CTLA4Ig/ Abatacept · 1 trial · 1 indication
| Name | Type | Description |
|---|---|---|
| CTLA4Ig / Abatacept | DRUG | - |
Inclusion Criteria: * Diagnosis and documentation of a history of stable psoriasis vulgaris of at least 6 months duration. * vulgaris total body surfae area involvement of at least 10% * Failure for toxicity and/or inefficacy of at least one standard anti- psoriatic therapy including topical treatm...
CTLA4Ig/Abatacept is an investigational drug being studied for the treatment of Psoriasis Vulgaris. It is being developed by Bristol-Myers Squibb Company (BMY) and is currently in Phase 2 clinical development. The drug has completed one clinical trial for this condition.
CTLA4Ig/Abatacept is a small molecule that targets CTLA4, a protein involved in immune response regulation. By modulating this target, the drug aims to affect the immune pathways implicated in Psoriasis Vulgaris. This mechanism is being evaluated in clinical trials for its potential therapeutic effect.
CTLA4Ig/Abatacept is being developed by Bristol-Myers Squibb Company, a biopharmaceutical company listed on the stock exchange under the ticker BMY. The company is conducting clinical research on this drug for the treatment of Psoriasis Vulgaris.
CTLA4Ig/Abatacept is in Phase 2 clinical development. It is an investigational drug, meaning it has not been approved by regulatory authorities and is still undergoing clinical trials to assess its safety and efficacy for the treatment of Psoriasis Vulgaris.
CTLA4Ig/Abatacept has one completed clinical trial, identified by the National Clinical Trial number NCT00287547. This was a Phase II randomized, double-blind, placebo-controlled study involving 144 patients with Psoriasis Vulgaris, conducted in the United States.
Yes, CTLA4Ig/Abatacept is also known as Abatacept. The drug is referred to by both names in clinical research. It is being studied under the name CTLA4Ig/Abatacept in the context of the Phase 2 trial for Psoriasis Vulgaris.