RecruitingPHASE1, PHASE2NCT05280509
Study of TL-895 Combined With Ruxolitinib in JAKi Treatment-Naïve MF Subjects and Subjects With MF Who Have a Suboptimal Response to Ruxolitinib
Studying Primary myelofibrosis
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Telios Pharma, Inc.
- Intervention
- TL-895(drug)
- Enrollment
- 70 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2022 – 2027
Study locations (19)
- University of Alabama at Birmingham, Birmingham, Alabama, United States
- Gabrail Cancer Center, Canton, Ohio, United States
- University of Cincinnati (UC), Cincinnati, Ohio, United States
- The University of Texas MD Anderson Cancer Center, Houston, Texas, United States
- CHU Angers, Angers, France
- AP-HM - Hôpital de la Timone, Marseille, France
- CHU de Nice - Hopital L'Archet II, Nice, France
- Hôpital Saint Louis - AP-HP, Paris, France
- Centre Hospitalier Lyon Sud, Pierre-Bénite, France
- Marien Hospital Duesseldorf, Düsseldorf, Germany
- Klinik fur Innere Medizin IV - Hamatologie/Onkologie, Universitatsklinikum Hall, Halle, Germany
- IRCCS Azienda Ospedaliero-Universitaria di Bologna - Policlinico di Sant'Orsola, Bologna, Italy
- Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico di Milano, Milan, Italy
- Azienda Ospedaliera di Perugia-Ospedale S. Maria della Misericordia, Perugia, Italy
- Pratia Onkologia Katowice, Katowice, Poland
- +4 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT05280509 on ClinicalTrials.govOther trials for Primary myelofibrosis
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