CLD-101 is under clinical development by Calidi Biotherapeutics and currently in Phase I for Gliosarcoma. According to GlobalData, Phase I drugs for Gliosarcoma 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 CLD-101 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.
CLD-101 overview
NNV1 is under development for the treatment of recurrent glioblastoma multiforme (GBM), anaplastic astrocytoma, gliosarcoma, anaplastic oligodendroglioma, anaplastic oligoastrocytoma, metastatic ovarian cancer, newly diagnosed high-grade glioma and recurrent high-grade glioma. The therapeutic candidate comprises immortalized neural stem cells (NSC) loaded with oncolytic adenovirus (CRAd-S-pk7). It is administered through intracerebral route and is being developed based on NeuroNova platform.
It was also under development for the treatment of malignant glioma.
Calidi Biotherapeutics overview
Calidi Biotherapeutics is an immuno-oncology company focusing on developing and commercializing efficient stem cell-based platforms for cancer treatment. The company is headquartered in San Diego, California, the US.
For a complete picture of CLD-101’s drug-specific PTSR and LoA scores, buy the report here.
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