RecruitingPhase 2NCT06854653
A Phase 2 Study of PTX 100 in Patients With Relapsed/Refractory CTCL
Studying Aggressive primary cutaneous T-cell lymphoma
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
- Prescient Therapeutics, Ltd.
- Intervention
- PTX-100(drug)
- Enrollment
- 115 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2025 – 2028
Study locations (15)
- City of Hope Comprehensive Cancer Cente, Duarte, California, United States
- University of California Irvine, Irvine, California, United States
- Yale Cancer Center, New Haven, Connecticut, United States
- Dana-Farber Cancer Institute, Boston, Massachusetts, United States
- Rochester Skin Lymphoma Medical Group. PLLC, Rochester, New York, United States
- Virginia Commonwealth University Massey Comprehensive Cancer Cente, Richmond, Virginia, United States
- Westmead Hospital, Westmead, New South Wales, Australia
- Epworth Healthcare, Melbourne, Victoria, Australia
- Linear Clinical Research, Nedlands, Western Australia, Australia
- CHU de Bordeaux - Hopital Saint André, Bordeaux, Bordeaux, France
- Hopital Lyon Sud, Lyon, Pierre-Benite, France
- Hopital Saint Louis, Paris, Île-de-France Region, France
- IRCCS Azienda Ospedaliero Universitaria di Bologna - Policlinico S. Orsola-Malpighi, Bologna, Bologna, Italy
- Universita degli Studi Di Brescia-Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia, Brescia, Brescia, Italy
- Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) - Ospedale San Raffaele (HSR) (Istituto Scientifico Universitario San Raffaele), Milan, Milano, Italy
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.
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