Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Propranolol Reactivation Mismatch (PRM) is an experimental therapeutic intervention developed by researchers at Massachusetts General Hospital for the treatment of post-traumatic stress disorder (PTSD). The protocol combines the pharmacological administration of propranolol, a non-selective beta-adrenergic receptor antagonist, with a behavioral memory reactivation technique. The intervention is based on the theory of memory reconsolidation, which posits that when a traumatic memory is retrieved, it enters a labile state (deconsolidation) before being stored again (reconsolidation). By introducing a 'mismatch'—a contextual discrepancy between the expected and actual experience during the trauma narrative reading—the memory is successfully deconsolidated. Propranolol is administered to block the noradrenergic activity necessary for the subsequent reconsolidation process, thereby reducing the emotional strength of the traumatic memory and alleviating PTSD symptoms.
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 Propranolol Reactivation Mismatch.