“Pivotal repeat-dose toxicity studies have been performed in mice (up to 3 months), rats (up to 6 months with a 3-month recovery period) and dogs (up to 12 months with a 13 weeks recovery period).”
Dog metabolism similar to human (limited hepatic metabolism, mostly renal excretion of parent); no unique human metabolite
“The in vivo metabolism profiles of solriamfetol are similar between dogs and humans, for which limited hepatic metabolism is observed and the majority of the drug is excreted unchanged in the urine.”
✓ VerifiedFDA pharmacology/toxicology review, p. 10Source ↗
Surrogate molecule
No surrogate; the clinical compound was tested
“Rats: In a pivotal 6-month repeat-dose toxicity study with a 3-month recovery period, daily oral doses of 29, 253 and 505 (reduced to 379 at study day 93 because of overt toxicity) mg/kg solriamfetol produced”
Rat (6-month) and dog (12-month); mouse up to 3 months
“Pivotal repeat-dose toxicity studies have been performed in mice (up to 3 months), rats (up to 6 months with a 3-month recovery period) and dogs (up to 12 months with a 13 weeks recovery period).”
“a complete battery of reproductive and developmental toxicology studies in the rat and/or rabbit”
✓ VerifiedFDA pharmacology/toxicology review, p. 123Source ↗
Species: carcinogenicity
Rat and mouse (2-year)
“Two-year carcinogenicity studies were conducted in rats and mice.”
✓ VerifiedFDA pharmacology/toxicology review, p. 2Source ↗
Surrogate used in
No surrogate used; solriamfetol tested directly
“Rats: In a pivotal 6-month repeat-dose toxicity study with a 3-month recovery period, daily oral doses of 29, 253 and 505 (reduced to 379 at study day 93 because of overt toxicity) mg/kg solriamfetol produced”