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Brief Title: Study of SyB C-1101 in Patients With Myelodysplastic Syndrome
Official Title: Multi-center, Open-label, Phase I Study of SyB C-1101 in Patients With Myelodysplastic Syndrome
Study ID: NCT03495167
Brief Summary: To assess tolerability of SyB C-1101 when administered orally BID for 21 days followed by a 7-day observation period in patients with recurrent/relapsed or refractory myelodysplastic syndrome in order to determine a recommended dose (RD). To assess safety, efficacy and pharmacokinetics.
Detailed Description:
Minimum Age: 20 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Research Site, Nagoya, Aichi, Japan
Research Site, Maebashi, Gunma, Japan
Research Site, Sapporo, Hokkaido, Japan
Research Site, Kobe, Hyogo, Japan
Research Site, Kurashiki, Okayama, Japan
Research Site, Shinagawa, Tokyo, Japan
Research Site, Fukuoka, , Japan
Research Site, Kumamoto, , Japan
Research Site, Kyoto, , Japan
Name: Katsuhisa Goto
Affiliation: SymBio Pharmaceuticals
Role: STUDY_DIRECTOR