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Набира участници Фаза 1 NCT05936359

A Study to Evaluate INCA033989 Administered as a Monotherapy or in Combination With Ruxolitinib in Participants With Myeloproliferative Neoplasms

Фаза 1 – тестване на безопасността при малка група хора
Заболявания: Myeloproliferative Neoplasms

Спонсор: Incyte Corporation

Налично на: БГ
Обобщение
This study is being conducted to evaluate the safety, tolerability, and dose-limiting toxicity (DLT) and determine the maximum tolerated dose (MTD) and/or recommended dose(s) for expansion (RDE) of INCA033989 administered as a monotherapy or in combination with ruxolitinib in participants with myeloproliferative neoplasms.
Кой може да участва
Inclusion Criteria: * Life expectancy \> 6 months. * Willingness to undergo a pretreatment and regular on-study BM biopsies and aspirates (as appropriate to disease). * Existing documentation from a qualified local laboratory of CALR exon-9 mutation. * Participants with MF and ET as defined in the protocol. Exclusion Criteria: * Presence of any hematological malignancy other than ET, PMF, or post-ET MF. * Active invasive malignancy over the previous 2 years. * Active HBV/HCV, HIV. * History of clinically significant or uncontrolled cardiac disease. * Has undergone any prior allogenic or autologous stem-cell transplantation or such transplantation is planned. * Laboratory values outside the Protocol-defined ranges. * Participants undergoing treatment with G-CSF, GM-CSF, or TPO-R agonists at any time within 4 weeks before the first dose of study treatment. * Prior history of major bleeding, or thrombosis within the last 3 months prior to study enrollment. * Any prior chemotherapy, immunomodulatory drug therapy, immunosuppressive therapy, biological therapy, endocrine therapy, targeted therapy, antibody, or hypomethylating agent used to treat the participant's disease within 5 half-lives or 28 days (whichever is shorter) before the first dose of study treatment. * For TGBs only: Undergoing treatment with a potent/strong inhibitor or inducer of CYP 3A4/5 within 14 days or 5 half-lives (whichever is longer) before the first dose of study treatment, or expected to receive such treatment during the study. Other protocol-defined Inclusion/Exclusion Criteria may apply.
Места на провеждане 8
Австралия (1)
Royal Brisbane and Women'S Hospital
Herston , Queensland
Канада (1)
Princess Margaret Cancer Center
Toronto , Ontario
Дания (1)
Odense University Hospital
Odense C
WITHDRAWN
Франция (1)
Institut Bergonie
Bordeaux
Италия (1)
Aou Policlinico S. Orsola-Malpighi
Bologna
Япония (1)
National Cancer Center Hospital East
Chiba-ken
Испания (1)
Hospital Universitario 12 de Octubre
Madrid
Великобритания (1)
Guys and St Thomas Nhs Foundation Trust
London
Технически детайли
Статус
Набира участници
Фаза
Фаза 1
Вид изследване
INTERVENTIONAL
Пол
Мъже и жени
Минимална възраст
18 Years
Здрави доброволци
Не
Начална дата
25.09.2023
Крайна дата
29.02.2028
Регистрационен номер
NCT05936359
Източник
anzctr
Запитване за медицински туризъм

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