Drugs / Cirtuvivint

Trials 6 · a red edge is where a trial was stopped

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 14 trials
Phase 1 NCT06856499 Dec 2025 → Jul 2027 expected fallopian tube cancer, ovarian endometrial cancer, primary peritoneal carcinoma University of Colorado, Denver Recruiting No outcome recorded
Phase 1 NCT06484062 Aug 2025 → Jun 2028 expected acute myeloid leukemia, myelodysplastic syndrome National Cancer Institute (NCI) Recruiting No outcome recorded
Phase 1 NCT05084859 Nov 2021 → Oct 2022 castration-resistant prostate carcinoma, colorectal cancer, non-small cell lung carcinoma Biosplice Therapeutics, Inc. Terminated No outcome recorded
Phase 1 NCT03355066 Nov 2017 → Nov 2022 cancer Biosplice Therapeutics, Inc. Terminated No outcome recorded
Phase 1/21 trial
Phase 1/2 NCT07155200 Dec 2025 → Jul 2028 expected small cell lung carcinoma Washington University School of Medicine Recruiting No outcome recorded
Phase 21 trial
Phase 2 NCT07032285 Jan 2025 → Apr 2027 expected soft tissue sarcoma Asociación Europea y Latinoamericana SELNET para la Investigación en Sarcomas Recruiting No outcome recorded

Evidence & citations 5 cited values

Every value below carries the sentence it was read from. 7 sources stand behind the page.

FieldValueCited text
Known as Cirtuvivint ClinicalTrials.gov intervention name — accepted as the source's own label NCT06856499
3

NCT07155200

NCT07032285

NCT06484062

Known as SM08502 “Cirtuvivint (SM08502) is a first in class pan CDC-like kinase (CLK) and dual specificity tyrosine kinase (DYRK) inhibitor with suspected multiple anti-tumor mechanisms of...” NCT06856499
3

“Cirtuvivint (SM08502) will be administered orally at 80 mg/day, 5 days on/2 days off.” NCT07032285

NCT05084859

NCT03355066

Action Inhibit “potent inhibition of CDC-like kinase (CLK) activity” PMID 31560935 Sep 2019
Modality Small molecule “SM08502, a novel small molecule in clinical development for the treatment of solid tumors” PMID 31560935 Sep 2019
Route Oral “SM08502 tablets to be administered orally.” NCT03355066