DelveInsight’s, “AL Amyloidosis Pipeline Insight 2023” report provides comprehensive insights about 10+ companies and 10+ pipeline drugs in the AL Amyloidosis pipeline landscape. It covers the AL Amyloidosis pipeline drug profiles, including AL Amyloidosis clinical trials and nonclinical stage products. It also covers the therapeutics assessment by product type, stage, route of administration, and molecule type. It further highlights the inactive pipeline products in this space.
Key Takeaways from the AL Amyloidosis Pipeline Report
To explore more information on the latest breakthroughs in the AL amyloidosis Pipeline treatment landscape of the report, click here @ AL amyloidosis Pipeline Outlook
AL amyloidosis Overview
Amyloid light-chain amyloidosis, (AL) is the most common form of systemic amyloidosis and is associated with an underlying plasma cell dyscrasia. AL amyloidosis is caused by a bone marrow disorder. The bone marrow in the center of bones produces cells in the blood system, including “plasma cells.”
Recent Developmental Activities in the AL Amyloidosis Treatment Landscape
For further information, refer to the detailed AL Amyloidosis Unmet Needs, AL Amyloidosis Market Drivers, and AL Amyloidosis Market Barriers, click here for AL Amyloidosis Ongoing Clinical Trial Analysis
AL Amyloidosis Emerging Drugs Profile
CAEL-101: Caelum Biosciences
CAEL-101 is a first-in-class anti-amyloid antibody designed to improve organ function by reducing or eliminating amyloid deposits in patients with amyloid light chain (AL) amyloidosis. Alexion is collaborating with Caelum Biosciences to develop CAEL-101 for light chain (AL) amyloidosis, a rare systemic disorder that causes misfolded immunoglobulin light chain protein to build up in and around tissues, resulting in progressive and widespread organ damage.
Ixazomib: Takeda
Ninlaro (ixazomib) is a proteasome inhibitor. Ixazomib preferentially binds and inhibits the chymotrypsin-like activity of the beta 5 subunit of the 20S proteasome. Ixazomib induced apoptosis of multiple myeloma cell lines in vitro. The drug is being evaluated in Phase III stage of development for the treatment of patients with AL Amyloidosis.
Belantamab mafodotin: GlaxoSmithKline
Belantamab mafodotin, or GSK2857916, is an afucosylated monoclonal antibody that targets B cell maturation antigen (BCMA) conjugated to the microtubule distrupter monomethyl auristatin-F (MMAF).1 Afucosylation of the Fc region of monoclonal antibodies enhances binding to the Fc region, which enhances antibody dependant cell mediated cytoxicity. Phase II clinical Study of Belantamab Mafodotin has been initiated to treat Patients with Relapsed or Refractory AL Amyloidosis.
STI 6129 : Sorrento Therapeutics
STI-6129 is an ADC with covalently bound duostatin tubulin inhibitors (Duostatin 5) using a proprietary site-specific C-LOCK™ chemical linker designed to reduce the premature systemic release of duostatin and avoid the potential for toxicity, particular ocular toxicity, seen with other ADCs, especially first-generation products. STI-6129 has demonstrated an improved therapeutic index in animal models, as compared to traditional non-selective conjugates.
AL Amyloidosis Pipeline Therapeutic Assessment
There are approx. 10+ key companies which are developing the therapies for AL Amyloidosis. The companies which have their A L Amyloidosis drug candidates in the most advanced stage, i.e. phase III include, Caelum Biosciences.
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Scope of the AL Amyloidosis Pipeline Report
Dive deep into rich insights for drugs for AL Amyloidosis Market Drivers and AL Amyloidosis Market Barriers, click here @ AL Amyloidosis Unmet Needs and Analyst Views
Table of Content
Got Queries? Find out the related information on AL Amyloidosis Mergers and acquisitions, AL Amyloidosis Licensing Activities @ AL Amyloidosis Emerging Drugs, and Recent Trends
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