PD-0299685

PD-0299685
Clinical data
Other namesPD-0299685; PD-299685; PD0299685; PD299685; PD-299,685
Routes of
administration
Oral[1]
Drug classGabapentinoid
ATC code
  • None
Identifiers
  • (3S,5R)-3-(aminomethyl)-5-methyloctanoic acid
CAS Number
PubChem CID
DrugBank
ChemSpider
UNII
ChEMBL
Chemical and physical data
FormulaC10H21NO2
Molar mass187.283 g·mol−1
3D model (JSmol)
  • CCC[C@@H](C)C[C@@H](CC(=O)O)CN
  • InChI=1S/C10H21NO2/c1-3-4-8(2)5-9(7-11)6-10(12)13/h8-9H,3-7,11H2,1-2H3,(H,12,13)/t8-,9+/m1/s1
  • Key:KKXFMWXZXDUYBF-BDAKNGLRSA-N

PD-0299685 is a gabapentinoid (α2δ subunit-containing voltage-gated calcium channel blocker) which was under development for the treatment of insomnia and vasomotor symptoms (hot flashes) related to menopause as well as interstitial cystitis.[1][2][3] It is taken orally.[1] PD-0299685 was under development by Pfizer.[1] It reached phase 2 clinical trials prior to the discontinuation of its development.[1]

See also

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References

[edit]
  1. ^ a b c d e "PD 0299685". AdisInsight. 5 November 2023. Retrieved 3 October 2025.
  2. ^ Lewis V (November 2009). "Undertreatment of menopausal symptoms and novel options for comprehensive management". Current Medical Research and Opinion. 25 (11): 2689–2698. doi:10.1185/03007990903240519. PMID 19775194.
  3. ^ Nickel JC, Crossland A, Davis E, Haab F, Mills IW, Rovner E, et al. (September 2012). "Investigation of a Ca2+ channel α2δ ligand for the treatment of interstitial cystitis: results of a randomized, double-blind, placebo controlled phase II trial". The Journal of Urology. 188 (3): 817–823. doi:10.1016/j.juro.2012.05.010. PMID 22818144.