
Curemark
Curemark | Novel Approaches to the Treatment of Neurological Diseases.
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$1.3m | Late VC | ||
Total Funding | 000k |
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Curemark is a private, clinical-stage biopharmaceutical company founded in 2007. The company focuses on the development of novel therapies to address unmet needs in neuro-developmental and neurological disorders. Its primary area of research is on treatments for autism and other conditions like ADHD and Fragile X syndrome.
The company's lead product candidate, CM-AT1, is a pancreatic replacement therapy designed to treat the core and non-core symptoms of autism in children. This therapy is based on the theory that a significant number of children with autism have a deficiency in the enzyme chymotrypsin, which is produced by the pancreas and is involved in protein digestion. The lack of this enzyme is believed to lead to a buildup of undigested protein, which can affect brain development and function. CM-AT1 aims to restore the normal digestive process, which has been shown in clinical trials to lead to long-term improvements in maladaptive behaviors in children with autism.
Curemark operates on a research and development-intensive business model. The company invests heavily in clinical trials to validate the safety and efficacy of its product candidates. Its primary clients would be patients diagnosed with the specific neurological disorders that its therapies target. The company collaborates with patient advocacy groups like the Autism Society of America to advance its research and raise awareness.
As a clinical-stage company, Curemark's revenue generation will likely depend on the successful commercialization of its products upon receiving regulatory approval. The company seeks funding and partnerships to support its research and development efforts and has presented its findings at major healthcare conferences to attract investment and collaborations.
Keywords: biopharmaceutical, neurological disorders, autism, clinical-stage, pancreatic replacement therapy, CM-AT1, neuro-developmental, ADHD, Fragile X syndrome, drug development