TTI-621 is under clinical development by Pfizer and currently in Phase II for Follicular Lymphoma. According to GlobalData, Phase II drugs for Follicular Lymphoma have a 43% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how TTI-621’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
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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.
TTI-621 overview
TTI-621 (SIRPa Fc) is under development for treatment of relapsed or refractory lymphomas, solid tumors, follicular lymphoma, primary mediastinal (thymic) large B-cell lymphoma and epithelioid sarcoma. It is administered through intratumoral and intravenous route. SIRPaFc (TTI-621) is a fusion protein that consists of the CD47-binding domain of human SIRPa linked to the Fc region of a human immunoglobulin (IgG1). The drug candidate targets CD47. It was also under development for the treatment of mycosis fungoides, Sezary syndrome, melanoma (intratumoral), relapsed or refractory lymphomas like indolent B-cell lymphoma, aggressive B-cell lymphoma, cutaneous T-cell lymphoma, peripheral T-cell lymphoma, chronic lymphocytic leukemia, multiple myeloma, acute myeloid leukemia, small cell lung cancer, acute lymphoblastic leukemia, myelodysplastic syndrome, myeloproliferative neoplasms, diffuse large B-cell lymphoma, solid tumors like leiomyosarcoma, soft-tissue sarcomas including high-grade leiomyosarcoma, undifferentiated pleomorphic sarcoma, myxofibrosarcoma, dedifferentiated liposarcoma, angiosarcoma,.
Pfizer overview
Pfizer discovers, develops, manufactures, and commercializes biopharmaceuticals. The company offers products to treat various conditions such as cardiovascular, metabolic and pain, women’s health, cancer, inflammation, immune disorders, and rare diseases. It also provides sterile injectable pharmaceuticals, biosimilars, active pharmaceutical ingredients (APIs) and contract manufacturing services. Pfizer sells its products through wholesalers, retailers, hospitals, individual provider offices, clinics, government agencies, and pharmacies. It has major manufacturing facilities in India, China, Japan, Ireland, Italy, Belgium, Germany, Singapore, and the US. The company provides its products in North America, South America, Asia-Pacific, Australia, Europe, Africa, and the Middle East. Pfizer is headquartered in New York, the US.
For a complete picture of TTI-621’s drug-specific PTSR and LoA scores, buy the report here.
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GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article.
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.
