Dalnicastobart is under clinical development by Lyvgen Biopharma and currently in Phase I for Advanced Malignancy. According to GlobalData, Phase I drugs for Advanced Malignancy does not have sufficient historical data to build an indication benchmark PTSR for Phase I. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the Dalnicastobart LoA Report. Buy the report here.
GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.
Dalnicastobart overview
Dalnicastobart (LVGN-7409) is under development for the treatment of solid tumors including lymphomas, non-small cell lung cancer, metastatic esophageal cancer, gastric cancer, metastatic head and neck carcinoma, metastatic hepatocellular carcinoma, metastatic ovarian carcinoma, metastatic soft tissue sarcoma and metastatic uveal melanoma. It is a humanized monoclonal antibody that acts by targeting CD40. It is administered through intravenous and oral route. The drug candidate is developed based on xLinkAb agonistic cross-linked antibody platform.
The drug candidate was under development for the treatment of triple negative breast cancer.
Lyvgen Biopharma overview
Lyvgen Biopharma, is a cancer immunotherapy service provider. The company is headquartered in China.
For a complete picture of Dalnicastobart’s drug-specific PTSR and LoA scores, buy the report here.
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