DelveInsight’s, “Follicular Lymphoma Pipeline Insight 2024” report provides comprehensive insights about 45+ companies and 50+ pipeline drugs in Follicular Lymphoma pipeline landscape. It covers the pipeline drug profiles, including clinical and nonclinical stage products. It also covers the Follicular Lymphoma therapeutics assessment by product type, stage, route of administration, and molecule type. It further highlights the inactive pipeline products in this space.
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Key Takeaways from the Follicular Lymphoma Pipeline Report
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Follicular Lymphoma Emerging Drugs Profile
MIL62 is a third-generation anti-CD20 antibody with a unique competitive position. MIL62 is the first domestically developed third-generation anti-CD20 antibody entering Phase III registration trial in China. MIL62 is self-developed by leveraging our ADCC-enhanced antibody platform. In in vitro and in vivo studies, MIL62 demonstrates stronger ADCC and anti-tumor activities than rituximab (first-generation anti-CD20 antibodies) and obinutuzumab (other third-generation anti-CD20 antibody). The company is implementing critical clinical development strategies to first pursue marketing approval from the NMPA for the treatment of relapsed and/or refractory FL patients and DLBCL patients. At the same time, MIL62 is being developed for previously untreated FL and DLBCL patients (a significantly larger patient population) by demonstrating clinical superiority over rituximab.
Loncastuximab tesirine-lpyl is an ADC composed of a humanized monoclonal antibody that binds to human CD19 and is conjugated through a linker to a PBD–dimer toxin. Once bound to a CD19-expressing cell, loncastuximab tesirine-lpyl is internalized into the cell, where enzymes release the PBD-based warhead. The warhead is designed to bind irreversibly to DNA to create highly potent interstrand cross-links that block DNA strand separation, thus disrupting essential DNA metabolic processes such as replication. This ultimately results in cell death. Currently, the drug is in Phase II stage of its clinical trial for the treatment of Follicular Lymphoma.
NX-2127 is an oral small molecule degrader of BTK and cereblon neosubstrates IKZF1 (Ikaros) and IKZF3 (Aiolos). Cereblon immunomodulatory drugs that induce degradation IKZF1 and IKZF3 such as lenalidomide and pomalidomide are FDA approved for a variety of hematologic malignancies including multiple myeloma, follicular lymphoma, and mantle cell lymphoma. We hypothesize that the combination of BTK degradation and cereblon immunomodulatory activity will have enhanced therapeutic benefit in patients suffering from a variety of B-cell malignancies. Currently, the drug is in Phase I stage of its clinical trial for the treatment of Follicular Lymphoma.
ABBV-319 is a novel oncology first-in-class steroid-based antibody-drug conjugate (ADC) targeting CD19 that is anticipated to have robust single-agent activity and provide significant clinical benefit as combination therapy in various B-cell malignancies, including diffuse large B-cell lymphoma (DLBCL), follicular lymphoma (FL), and chronic lymphocytic leukemia (CLL). The mechanism of action involves the ADC binding to CD19 on the surface of B-cell cancer cells, followed by internalization into the cells through receptor-mediated endocytosis. Once inside, the linker component of the ADC is cleaved, releasing the cytotoxic drug payload, which then targets and kills the cancer cells. Currently, the drug is in Phase I stage of its clinical trial for the treatment of Follicular Lymphoma.
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Follicular Lymphoma pipeline report provides the therapeutic assessment of the pipeline drugs by the Route of Administration
Follicular Lymphoma Products have been categorized under various Molecule types such as
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Scope of the Follicular Lymphoma Pipeline Report
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