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| Other names | CVL-865; PF-06372865; PF-6372865 |
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Routes of administration | Oral administration |
| Drug class | GABAA receptor positive allosteric modulator |
| Pharmacokinetic data | |
| Metabolism | CYP3A4 [1] |
| Elimination half-life | 11 hours [1] |
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| Chemical and physical data | |
| Formula | C22H21FN4O3S |
| Molar mass | 440.49 g·mol−1 |
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Darigabat (developmental code names CVL-865, PF-06372865, PF-6372865) is a GABAergic medication which is under development for the treatment of photosensitive epilepsy, focal onset seizures, panic disorder, and other anxiety disorders. [2] [3] It was also under development for the treatment of generalized anxiety disorder and chronic lower back pain, but development for these indications was discontinued. [2] [3] [4] It is taken via oral administration. [2]
Darigabat acts as a GABAA receptor positive allosteric modulator [2] [3] [5] It is specifically a positive allosteric modulator that selectively targets α2, α3, and α5 subunit-containing GABAA receptors, with minimal functional activity at α1 subunit-containing GABAA receptors. [3] [5] A dose of darigabat that achieved more than 80% receptor occupancy showed no somnolence with dose titration, whereas benzodiazepines, which are non-selective GABAA receptor positive allosteric modulators, achieve only 10 to 15% receptor occupancy whilst producing significant or severe somnolence. [3] [5] It is theorized that α1 subunit-containing GABAA receptors preferentially mediate sedation, amnesia, and ataxia, whereas α2 and α3 subunit-containing GABAA receptors mediate anxiolysis. [3] [5] However, this model has also been questioned. [4] α1 subunit-containing GABAA receptors are said to be completely unaffected by darigabat. [6] The elimination half-life of darigabat is 11 hours and it is metabolized mainly by CYP3A4. [1]
In clinical trials conducted thus far, side effects of darigabat have included dizziness, fatigue, headache, mild-to-moderate somnolence, bradyphrenia (slowness of thought), modest memory impairment, mild cognitive impairment, balance impairment, and feeling abnormal. [3] [6] It has been described as well-tolerated. [3] [4]
Darigabat was originated by Pfizer and is under development by Cerevel Therapeutics and Pfizer. [2] As of January 2023, it is in phase 2 clinical trials for epilepsy and seizures, phase 1 trials for panic disorder, and preclinical development for anxiety disorders. [2] [3] Development for back pain was discontinued due to lack of effectiveness in a phase 2 trial, while development for generalized anxiety disorder was discontinued due to business reasons as well as lack of effectiveness in a phase 2 trial. [3] [4] [2]
See also
References
- ^ a b c Elkommos S, Mula M (December 2022). "Current and future pharmacotherapy options for drug-resistant epilepsy". Expert Opin Pharmacother. 23 (18): 2023–2034. doi: 10.1080/14656566.2022.2128670. PMID 36154780. S2CID 252542159.
- ^ a b c d e f g "Darigabat - Cerevel Therapeutics - AdisInsight".
- ^ a b c d e f g h i j Cerne R, Lippa A, Poe MM, Smith JL, Jin X, Ping X, Golani LK, Cook JM, Witkin JM (June 2022). "GABAkines - Advances in the discovery, development, and commercialization of positive allosteric modulators of GABAA receptors". Pharmacol Ther. 234: 108035. doi: 10.1016/j.pharmthera.2021.108035. PMC 9787737. PMID 34793859.
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- ^ a b c d Quagliato LA, Carta MG, Nardi AE (2022). "Panic Disorder Seeks More Specific Drugs for Treatment: Might the Amygdala Be the Best Target?". J Clin Psychopharmacol. 42 (5): 427–428. doi: 10.1097/JCP.0000000000001591. PMID 36099401. S2CID 252219658.
- ^ a b Janković SM, Dješević M, Janković SV (2021). "Experimental GABA A Receptor Agonists and Allosteric Modulators for the Treatment of Focal Epilepsy". J Exp Pharmacol. 13: 235–244. doi: 10.2147/JEP.S242964. PMC 7954424. PMID 33727865.