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List of investigational anxiety disorder drugs

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This is a list of investigational anxiety disorder drugs, or drugs that are currently under development for clinical use in the treatment of anxiety disorders (type unspecified) but are not yet approved.

Contents

Chemical/generic names are listed first, with developmental code names, synonyms, and brand names in parentheses. The format of list items is "Name (Synonyms) – Mechanism of Action [Reference]".

This list was last comprehensively updated in September 2025. It is likely to become outdated with time.

Under development

Phase 3

Phase 2

Phase 1

Preclinical

Phase unknown

Not under development

No development reported

Discontinued

Clinically used drugs

Approved drugs

See also

References

  1. Robison R, Barrow R, Conant C, Foster E, Freedman JM, Jacobsen PL, Jemison J, Karas SM, Karlin DR, Solomon TM, Halperin Wernli M, Fava M (September 2025). "Single Treatment With MM120 (Lysergide) in Generalized Anxiety Disorder: A Randomized Clinical Trial". JAMA. doi:10.1001/jama.2025.13481. PMID   40906494.
  2. "BAER 101". AdisInsight.
  3. 1 2 Maramai S, Benchekroun M, Ward SE, Atack JR (April 2020). "Subtype Selective γ-Aminobutyric Acid Type A Receptor (GABAAR) Modulators Acting at the Benzodiazepine Binding Site: An Update". J Med Chem. 63 (7): 3425–3446. doi:10.1021/acs.jmedchem.9b01312. hdl: 11365/1214874 . PMID   31738537.
  4. Chen X, Jacobs G, de Kam M, Jaeger J, Lappalainen J, Maruff P, Smith MA, Cross AJ, Cohen A, van Gerven J (December 2014). "The central nervous system effects of the partial GABA-Aα2,3 -selective receptor modulator AZD7325 in comparison with lorazepam in healthy males". Br J Clin Pharmacol. 78 (6): 1298–1314. doi:10.1111/bcp.12413. PMC   4256620 . PMID   24802722.
  5. Roberti R, De Caro C, Iannone LF, Zaccara G, Lattanzi S, Russo E (June 2021). "Pharmacology of Cenobamate: Mechanism of Action, Pharmacokinetics, Drug-Drug Interactions and Tolerability". CNS Drugs. 35 (6): 609–618. doi:10.1007/s40263-021-00819-8. PMID   33993416.
  6. Cross, Ryan (19 August 2025). "Exclusive: Sensorium raises $25M to test succulent-derived drug for anxiety". Endpoints News. The company zeroed in on a molecule derived from a South African succulent known to scientists as Sceletium tortuosum and commonly referred to as kanna. [...] the company's drug "was inspired by a unique natural product found among the diverse molecules," but did not confirm if it came from mesembrine. Chewing kanna is linked to rapid calming action within 30 to 60 minutes, [...] Other researchers have previously shown that kanna inhibits the serotonin transporter, an important protein that moves serotonin in and out of the junctions between brain cells. Antidepressants called selective serotonin reuptake inhibitors (SSRIs) also block the serotonin transporter, but typically take four to six weeks for their effects to kick in, creating a puzzle about why the succulent compound worked so quickly. "We were convinced, quite frankly, that it must be hitting some target that we don't know about," Hooker said. "And we went deep. We looked at many hundreds, if not a thousand or more targets." It turned out that the molecule was binding to the serotonin transporter — a bit of a disappointment at first, given the startup's novel mechanism mandate. However, while SSRIs directly block the ability of serotonin to bind to the transporter, Hooker said he was surprised to find that Sensorium's compound binds to a different site on the protein that doesn't compete with serotonin binding. Hooker is writing a paper to describe the mechanism in more detail. The company is also still trying to figure out exactly why touching the transporter differently has such a seemingly rapid action. Early work suggests it is rooted in downstream signaling proteins called kinases that "fundamentally tune the circuit differently," he said. [...] Sensorium has created hundreds of derivatives of the natural molecule to make a version dubbed SNTX-2643, which can be taken orally once a day. Hooker hopes it will provide an alternative to anxiety medications, including SSRIs and benzodiazepines. Hooker declined to say when the Phase 1 study would wrap up.
  7. Galambos J, Domány G, Nógrádi K, Wágner G, Keserű GM, Bobok A, Kolok S, Mikó-Bakk ML, Vastag M, Sághy K, Kóti J, Szakács Z, Béni Z, Gál K, Szombathelyi Z, Greiner I (February 2016). "4-Aryl-3-arylsulfonyl-quinolines as negative allosteric modulators of metabotropic GluR5 receptors: From HTS hit to development candidate". Bioorg Med Chem Lett. 26 (4): 1249–1252. doi:10.1016/j.bmcl.2016.01.024. PMID   26774652.
  8. Matier WL, Patil G (2000). "Esprolol hydrochloride: a new beta adrenergic antagonist with a rapid onset of effect". Heart Dis. 2 (2): 146–150. PMID   11728252.
  9. Zuiker RG, Chen X, Østerberg O, Mirza NR, Muglia P, de Kam M, Klaassen ES, van Gerven JM (March 2016). "NS11821, a partial subtype-selective GABAA agonist, elicits selective effects on the central nervous system in randomized controlled trial with healthy subjects". J Psychopharmacol. 30 (3): 253–262. doi:10.1177/0269881115620435. PMID   26655084.
  10. "Tiagabine". AdisInsight. 24 October 2021. Retrieved 17 January 2026.
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