Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
SEAD1 is a synthetic peptide therapeutic designed to mimic the soluble form of the brain protein α2δ-1 (encoded by the *Cacna2d1* gene). Developed by researchers at Northwestern University, it aims to treat the cognitive symptoms of schizophrenia and other neuropsychiatric disorders. The mechanism involves restoring network homeostasis in brain circuits that become overexcited due to a deficiency of naturally occurring soluble α2δ-1 in the cerebrospinal fluid. In preclinical studies, SEAD1 administration corrected abnormal brain circuit activity and rescued behavioral deficits in mouse models of schizophrenia without causing common side effects like sedation. The therapeutic is currently being optimized for clinical trials, particularly for patients with 16p11.2 duplication syndrome.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on SEAD1.