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.

Geptanolimab overview

Geptanolimab (CBT-501) is under development for the treatment of cancers such as melanoma, renal cell carcinoma, head and neck cancer, bladder cancer, ovarian cancer, colorectal cancer, gastric cancer, soft tissue sarcoma, ALK-negative anaplastic large cell lymphoma, endometrial cancer, metastatic cervical cancer, spongioblastoma, non-small cell lung cancer, mesothelioma, esophageal cancer, nasopharyngeal cancer, gastroesophageal junction adenocarcinoma and lymphomas including classical Hodgkin lymphoma, peripheral T-cell lymphoma, NK-T cell lymphoma and mediastinal B cell lymphoma. It is administered through intravenous infusion. The drug candidate is an IgG4 humanized monoclonal antibody against programmable death-1 (PD-1).

It was also under development for the treatment of metastatic hepatocellular carcinoma, thymic carcinoma and metastatic renal cell carcinoma.

Apollomics overview

Apollomics formerly CBT Pharmaceuticals, is a biotechnology company that discovers and develops oncology therapies. It is investigating APL-101, a novel small molecule c-Met inhibitor (c-METi) that targets the c-Met-dysregulated pathway in gastric, hepatic, pancreatic and lung tumors; and APL-102, an oral multi kinase inhibitor (mKi) targeting receptor tyrosine kinase (RTKs) and serine or threonine-kinases in liver, breast, colorectal, gastric cancers. The company is also evaluating APL-106 against acute myeloid leukemia (AML); APL-108 to treat multiple myeloma (MM); APL-501 and APL-102 targeting solid tumors; APL-502 and APL-801 against multiple tumors; and APL-810 for gastroenterological cancers. It operates in Taiwan and the US. Apollomics is headquartered in Pleasanton, California, the US.

For a complete picture of Geptanolimab’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 2 September 2023

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GlobalData’s Likelihood of Approval analytics tool dynamically assesses and predicts how likely a drug will move to the next stage in clinical development (PTSR), as well as how likely the drug will be approved (LoA). This is based on a combination of machine learning and a proprietary algorithm to process data points from various databases found on GlobalData’s Pharmaceutical Intelligence Center.