The most commonly used efficacy endpoints in clinical trials of anti-tumor drugs are Overall Survival (OS), Objective Response Rate (ORR), and Progression Free Survival (PFS), among others.
Ocular Therapeutix has publicized the start of its premiere primary clinical trial to examine OTX-TKI, a proprietary axitinib intravitreal implant, for tackling wet age-related macular degeneration.
This article summarized the latest R&D progress of cysteamine hydrochloride, the Mechanism of Action for cysteamine hydrochloride, and the drug target R&D trends for cysteamine hydrochloride.
Eli Lilly along with POINT Biopharma Global, Inc. have declared a final agreement where Lilly will take over POINT, a company specializing in radiopharmaceuticals.
TTF, in comparison to PFS, synthesizes the effectiveness and safety characteristics of the drug, encompasses treatment failure for any reason and includes death.
This article summarized the latest R&D progress of cyclizine hydrochloride, the Mechanism of Action for cyclizine hydrochloride, and the drug target R&D trends for cyclizine hydrochloride.
Event-Free Survival (EFS), compared to Disease-Free Survival (DFS), adds a surgical intervention criterion and is often used to evaluate neoadjuvant therapy pre-surgery, or radiotherapy.
Disease Control Rate refers to the proportion of patients who, according to internationally recognized criteria for alleviating evaluation, achieve tumor relief (PR+CR) and stable disease (SD) after treatment and can maintain for the minimum duration requirement.
This article summarized the latest R&D progress of choline alfoscerate, the Mechanism of Action for choline alfoscerate, and the drug target R&D trends for choline alfoscerate.
PFS is a tumor measurement-based endpoint that primarily evaluates the anti-tumor activity of a drug and, to a certain extent, considers the drug's safety and patient survival (accidental death).