Article · Wikipedia archive · Last revised Jul 10, 2026

ML-007

ML-007 is a selective muscarinic acetylcholine M1 and M4 receptor agonist which is under development for the treatment of schizophrenia, psychotic disorders, and dyskinesias. It is being developed in combination with a peripherally selective muscarinic acetylcholine receptor antagonist (also known as ML-007/peripherally acting anticholinergic or ML-007/PAC). The drug is taken orally.

Last revised
Jul 10, 2026
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≈ 1 min
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332 w
Citations
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Source
ML-007
Clinical data
Other namesML007; ML-007/PAC; ML007/PAC
Routes of
administration
Oral1
Drug classMuscarinic acetylcholine M1 and M4 receptor agonist1

ML-007 is a selective muscarinic acetylcholine M1 and M4 receptor agonist which is under development for the treatment of schizophrenia, psychotic disorders, and dyskinesias.123456 It is being developed in combination with a peripherally selective muscarinic acetylcholine receptor antagonist (also known as ML-007/peripherally acting anticholinergic or ML-007/PAC).254 The drug is taken orally.1

It produces antipsychotic-like effects in rodents, including inhibition of amphetamine and phencyclidine (PCP)-induced hyperlocomotion and activity in the conditioned avoidance response test.6 These effects appear to dependent on activation of both muscarinic acetylcholine M1 and M4 receptors.6 The drug is approximately 10-fold more potent than xanomeline in these tests.6

As of January 2024, ML-007 is in phase 1 clinical trials for schizophrenia, psychotic disorders, and dyskinesias.134 It is under development by MapLight Therapeutics.13 The drug is a small molecule, but its chemical structure does not seem to have been disclosed.513

See also

See also

References

References

  1. "ML 007". AdisInsight. Springer Nature Switzerland AG. 9 January 2024. Retrieved 21 October 2024.
  2. "ML 007/muscarinic antagonist". AdisInsight. 8 May 2026. Retrieved 7 June 2026.
  3. "Delving into the Latest Updates on ML-007 with Synapse". Synapse. 19 September 2024. Retrieved 21 October 2024.
  4. Yohn SE, Harvey PD, Brannan SK, Horan WP (4 October 2024). "The potential of muscarinic M1 and M4 receptor activators for the treatment of cognitive impairment associated with schizophrenia". Frontiers in Psychiatry. 15. Frontiers Media SA. doi:10.3389/fpsyt.2024.1421554. ISSN 1664-0640. PMC 11525114. PMID 39483736.
  5. Walker LC, Huckstep KL, Becker HC, Langmead CJ, Lawrence AJ (November 2024). "Targeting muscarinic receptors for the treatment of alcohol use disorders: Opportunities and hurdles for clinical development". British Journal of Pharmacology. 181 (22): 4385–4398. doi:10.1111/bph.16081. PMID 37005377.
  6. Chatterjee S, Soria M, Norville ZC, Thompson KR, Lillie J, Kreitzer AC, et al. (April 2026). "Preclinical efficacy of the muscarinic agonist ML-007 in psychosis models depends on both M1 and M4 receptors". Neuropsychopharmacology. 51 (5): 840–845. doi:10.1038/s41386-025-02256-3. PMC 13013942. PMID 41046244.