Saint Vincent's Hospital |
Darlinghurst, New South Wales, Australia, 2010 |
Royal Adelaide Hospital |
Adelaide, South Australia, Australia, 5000 |
Peninsula Private Hospital |
Frankston, Victoria, Australia, 3199 |
Eastern Health Clinical School |
Box Hill, Australia, 3128 |
Alfred Hospital |
Melbourne, Australia, 3004 |
Medical University of Graz |
Graz, Austria, A-8036 |
Medical University Innsbruck |
Innsbruck, Austria, 6020 |
Elisabethinen Hospital Linz |
Linz, Austria, 4020 |
Salzburger Landkliniken St. Johanns-Spital |
Salzburg, Austria, 5020 |
Medical University of Vienna |
Vienna, Austria, 1090 |
Klinikum Wels-Grieskirchen GmbH |
Wels, Austria, 4600 |
Hanusch Krankenhaus |
Wien, Austria, 1140 |
AZ Sint-Jan AV Brugge |
Brugge, Belgium, 8000 |
Cliniques Universitaires Saint-Luc |
Bruxelles, Belgium, 1200 |
Centre Hospitalier de Jolimont-Lobbes |
La Louvière-(Haine St-Paul), Belgium, 7100 |
UZ Leuven |
Leuven, Belgium, 3000 |
Centre Hospitalier Universitaire de Liege - Sart Tilman |
Liege, Belgium, 4000 |
Cliniques Universitaires UCL de Mont-Godine |
Yvoir, Belgium, 5530 |
Peking University People's Hospital |
Beijing, China, 100044 |
Peking Union Medical College Hospital |
Beijing, China, 100730 |
Fujian Medical University Union Hospital |
Fuzhou, China, 350001 |
Guangdong General Hospital |
Guangzhou, Guangdong, China, 510080 |
Jiangsu Province Hospital, The First Affiliated Hospital of Nanjing Medical University |
Nanjing, China, 210029 |
Chinese Academy of Medical Sciences & Peking Union Medical College |
Tianjin, China, 300041 |
Henan Cancer Hospital |
Zhengzhou, China |
Fakultni Nemocnice Brno |
Brno, Czechia, 625 00 |
Fakultni Nemocnice Ostrava |
Ostrava-Poruba, Czechia, 708 52 |
Vseobecna Fakultni Nemocnice v Praze |
Prague 2, Czechia, 128 08 |
CHU d'Angers |
Angers, France, 49033 |
CHRU de Brest - Hopital Morvan |
Brest, France, 29200 |
Centre Hospitalier de Lens |
Lens Cedex, France, 62307 |
CHRU Claude Huriez |
Lille, France, 59037 |
CHU Nice Hopital de L'Archet 2 |
Nice Cedex 3, France, 06200 |
Centre Hospitalier Universitaire de Nimes - Hopital Universitaire Caremeau |
Nimes Cedex 9, France, 30029 |
Hopital Saint Louis |
Paris, France, 75010 |
CHRU - Hopital du Haut Leveque |
Pessac, France, 33604 |
Centre Hospitalier Lyon Sud - Hospices Civils de Lyon Groupement Hospitalier Sud |
Pierre-Benite, France, 69495 |
CHU La Miletrie |
Poitiers Cedex, France, 86021 |
CHU Strasbourg - Hopital Civil |
Strasbourg, France, 67091 |
Institut Universitaire du Cancer de Toulouse - Oncopole |
Toulouse Cedex 9, France, 31059 |
Unviversitatsklinikum Aachen |
Aachen, Germany, 52074 |
Klinikum der Johann Wolfgang Goethe Universitat |
Frankfurt am Main, Germany, 60590 |
Universitaetsklinikum Halle Saale |
Halle, Germany, 06120 |
Universitaetsklinikum Jena |
Jena, Germany, 07747 |
Universitaetsklinikum Magdeburg A oeR |
Magdeburg, Germany, 39120 |
University of Heidelberg - Universitatsklinikum Mannheim |
Mannheim, Germany, 68167 |
Johannes Wiesling Klinikum Minden |
Minden, Germany, 32429 |
TU München - Klinikum rechts der Isar |
München, Germany, 81675 |
Universitaetsklinikum Ulm |
Ulm, Germany, 89081 |
Semmelweis Egyetem |
Budapest, Hungary, 1088 |
Petz Aladar Megyei Oktato Korhaz |
Gyor, Hungary, 9023 |
Somogy Megyei Kaposi Mor Oktato Korhaz |
Kaposvar, Hungary, 7400 |
SzSzB Megyei Korhazak es Egyetemi Oktatokorhaz |
Nyiregyhaza, Hungary, 4400 |
Szegedi Tudomanyegyetem - Szent-Gyorgyi Albert Klinikai Kozpont |
Szeged, Hungary, 6720 |
Cork University Hospital |
Cork, Ireland |
Mater Misericordiae University Hospital |
Dublin, Ireland, Dublin 7 |
St. James' Hospital |
Dublin, Ireland, Dublin 8 |
A.O.U. di Bologna Policlinico S.Orsola-Malpighi |
Bologna, Italy, 40138 |
ASST Spedali Civili P.O. di Brescia |
Brescia, Italy, 25123 |
Azienda Ospedaliero - Universitaria Policlinico - Vittorio Emanuele - Ospedale Gaspare Rodolico |
Catania, Italy, 95123 |
Azienda Ospedaliero-Universitaria Careggi |
Firenze, Italy, 50134 |
IRCSS Ospedale Maggiore Policlinico, Mangiagalli e Regina Elena |
Milano, Italy, 20122 |
Ospedale Cardarelli |
Naples, Italy, 80131 |
Fondazione IRCCS Policlinico San Matteo |
Pavia, Italy, 27100 |
Policlinico Umberto I - Universita La Sapienza |
Roma, Italy, 00168 |
Universita Cattololica del Sacro Cuore |
Roma, Italy, 00168 |
Azienda Ospedaliera S. Andrea - Università La Sapienza |
Roma, Italy, 00189 |
Azienda Ospedaliera Citta della Salute e della Scienza di Torino |
Torino, Italy, 10126 |
Azienda Ospedaliero-Universitaria Santa Maria della Misericordia die Udine |
Udine, Italy, 33100 |
Universita degli Studi dell'Insubria - Ospedale di Circolo e Fondazione Macchi - Varese |
Varese, Italy, 21100 |
Azienda Ospedaliera Universitaria Integrata di Verona |
Verona, Italy, 37134 |
Seoul National University Bundang Hospital |
Seongnam-si, Korea, Republic of, 13620 |
Samsung Medical Center |
Seoul, Korea, Republic of, 06351 |
Seoul St Marys Hospital College of Medicine The Catholic University of Korea |
Seoul, Korea, Republic of, 137-701 |
Soon Chun Hyang University Hospital Seoul |
Seoul, Korea, Republic of, 140-887 |
Seoul National University Hospital |
Seoul, Korea, Republic of, 3080 |
Asan Medical Center |
Seoul, Korea, Republic of, 5505 |
UMC Maastricht |
Maastricht, Netherlands, 6229 HX |
Radboud University Medical Center |
Nijmegen, Netherlands, 6525 GA |
Szpital Kliniczny im. H.Swiecickiego Uniwersytetu Medycznego im. Karola Marcinkowskiego w Poznaniu |
Poznan, Poland, 60-569 |
Instytut Hematologii i Transfuzjologii w Warszawie |
Warszawa, Poland, 02-776 |
Akademicki Szpital Kliniczny im. Jana Mikulicza-Radeckiego |
Wroclaw, Poland, 50-556 |
FSBI Hematology Research Center Ministry of Healthcare of the Russian Federation |
Moscow, Russian Federation, 125167 |
Moscow State Healthcare Institution City clinical hospital n.a. S.P.Botkin |
Moscow, Russian Federation, 125284 |
City Clinical Hospital 40 |
Moscow, Russian Federation, 129301 |
Novosibirsk State Medical University (NSMU) |
Novosibirsk, Russian Federation, 630066 |
Russian Research Institute of Hematology and Transfusiology of the Federal Biomedical Agency |
Saint Petersburg, Russian Federation, 191024 |
Pavlov First Saint Petersburg State Medical University |
Saint-Petersburg, Russian Federation, 197022 |
Federal Centre of Heart, Blood and Endocrinology of Rosmed technlologies V.A. Almazov |
St Petersburg, Russian Federation, 197341 |
State Budgetary Healthcare Organization |
Vladikavkaz, Russian Federation, 362002 |
Complejo Hospitalario Universitario A Coruna |
May 6, 2019
|
May 16, 2019
|
April 8, 2021
|
September 9, 2019
|
February 24, 2022 (Final data collection date for primary outcome measure)
|
Proportion of subjects who have ≥ 35% SVR at end of cycle 6 [ Time Frame: At the end of Cycle 1 (each cycle is 28 days) ] Spleen volume response rate (RR)
|
Same as current
|
|
- Proportion of subjects with ≥ 50% reduction in total symptom scores measured by MFSAF at end of cycle 6 [ Time Frame: Up to end of Cycle 6 (each cycle is 28 days) ]
Symptom response rate (SRR)
- Proportion of subjects who have ≥ 25% reduction in spleen volume at the end of cycle 6 [ Time Frame: At the end of Cycle 1 (each cycle is 28 days) ]
Spleen volume response rate (RR25)
- Adverse Events (AEs) [ Time Frame: Up to 30 days post last dose ]
Number of participants with adverse event
- Proportion of subjects who have ≥ 50% reduction in spleen size by palpation at end of cycle 6 [ Time Frame: Up to end of Cycle 6 (each cycle is 28 days) ]
Spleen response rate by palpation (RRP)
- Durability of Spleen Volume Response by MRI/CT (DR) [ Time Frame: Up to end of Cycle 6 (each cycle is 28 days) ]
Is defined as time from the first documented spleen response (ie, ≥ 35% reduction in spleen volume) to the first documented spleen volume reduction < 35%.
- Duration of ≥ 50 % reduction in spleen size by palpation for subjects with a palpable spleen at least 5 cm below the left costal margin (LCM) at baseline [ Time Frame: Up to approximately 30 months ]
From C1D1 until the 30- day follow-up after last dose visit
- Duration of ≥ 50% reduction in total symptom scores measured by MFSAF [ Time Frame: From enrollment until 30 days post last dose ]
Durability of symptoms response (DSR)
- Time from randomization to death due to any reason or disease progression (modified IWG-MRT 2013 including ≥ 25% increase in spleen volume by MRI/CT) [ Time Frame: Up to 24 months from enrollment to End of Survival Follow-up ]
Spleen and disease progression free survival (SDPFS)
- Gastrointestinal Adverse Events [ Time Frame: Up to approximately 30 months ]
Incidence of subjects with Grade 3 or higher Gastrointestinal events (nausea, diarrhea, or vomiting) according to CTCAE v5.0
- Encephalopathy Events, including Wernicke's [ Time Frame: Up to 30 days post last dose ]
Occurrence of confirmed encephalopathy events, including Wernicke's
- Health-Related Quality of Life (HRQoL) [ Time Frame: Up to 30-day follow-up after last dose visit ]
To evaluate Health-Related Quality of Life (HRQoL) as measured by the European Organization for Research and Treatment of Cancer Quality of Life C30 (EORTC QLQ-C30)
- EQ-5D-5L [ Time Frame: Up to 20-day follow-up after last dose visit ]
To evaluate Patient Reported Outcomes (PRO) as measured by the EQ-5D-5L questionnaire
- Overall Survival (OS) [ Time Frame: From randomization to the End of Survival Follow-up (approximately 12 months) ]
Time from randomization to death due to any reason
|
- Proportion of subjects with ≥ 50% reduction in total symptom scores measured by MFSAF at end of cycle 6 [ Time Frame: Up to end of Cycle 6 (each cycle is 28 days) ]
Symptom response rate (SRR)
- Proportion of subjects who have ≥ 25% reduction in spleen volume at the end of cycle 6 [ Time Frame: At the end of Cycle 1 (each cycle is 28 days) ]
Spleen volume response rate (RR25)
- Adverse Events (AEs) [ Time Frame: Up to 30 days post last dose ]
Number of participants with adverse event
- Proportion of subjects who have ≥ 50% reduction in spleen size by palpation at end of cycle 6 [ Time Frame: Up to end of Cycle 6 (each cycle is 28 days) ]
Spleen response rate by palpation (RRP)
- Durability of Spleen Volume Response by MRI/CT (DR) [ Time Frame: Up to end of Cycle 6 (each cycle is 28 days) ]
Is defined as time from the first documented spleen response (ie, ≥ 35% reduction in spleen volume) to the first documented spleen volume reduction < 35%.
- Duration of ≥ 50 % reduction in spleen size by palpation for subjects with a palpable spleen at least 5 cm below the left costal margin (LCM) at baseline [ Time Frame: Up to approximately 30 months ]
From C1D1 until the 30- day follow-up after last dose visit
- Duration of ≥ 50% reduction in total symptom scores measured by MFSAF [ Time Frame: From enrollment until 30 days post last dose ]
Durability of symptoms response (DSR)
- Time from randomization to death due to any reason or disease progression (modified IWG-MRT 2013 including ≥ 25% increase in spleen volume by MRI/CT) [ Time Frame: Up to 24 months from enrollment to End of Survival Follow-up ]
Spleen and disease progression free survival (SDPFS)
- Gastrointestinal Adverse Events [ Time Frame: Up to approximately 30 months ]
Incidence of subjects with Grade 3 or higher Gastrointestinal events (nausea, diarrhea, or vomiting) according to CTCAE v5.0
- Wernicke encephalopathy (WE) events [ Time Frame: Up to 30 days post last dose ]
Occurrence of confirmed Wernicke encephalopathy events
- Health-Related Quality of Life (HRQoL) [ Time Frame: Up to 30-day follow-up after last dose visit ]
To evaluate Health-Related Quality of Life (HRQoL) as measured by the European Organization for Research and Treatment of Cancer Quality of Life C30 (EORTC QLQ-C30)
- EQ-5D-5L [ Time Frame: Up to 20-day follow-up after last dose visit ]
To evaluate Patient Reported Outcomes (PRO) as measured by the EQ-5D-5L questionnaire
- Overall Survival (OS) [ Time Frame: From randomization to the End of Survival Follow-up (approximately 12 months) ]
Time from randomization to death due to any reason
|
Not Provided
|
Not Provided
|
|
An Efficacy and Safety Study of Fedratinib Compared to Best Available Therapy in Subjects With DIPSS-intermediate or High-risk Primary Myelofibrosis, Post-polycythemia Vera Myelofibrosis, or Post-essential Thrombocythemia Myelofibrosis and Previously Treated With Ruxolitinib
|
A Phase 3, Multicenter, Open-label, Randomized Study to Evaluate the Efficacy and Safety of Fedratinib Compared to Best Available Therapy (BAT) in Subjects With DIPSS (Dynamic International Prognostic Scoring System)-Intermediate or High-risk Primary Myelofibrosis (PMF), Post-polycythemia Vera Myelofibrosis (Post-PV MF), or Post-essential Thrombocythemia Myelofibrosis (Post-ET MF) and Previously Treated With Ruxolitinib
|
A Phase 3, multicenter, open-label, randomized study to evaluate the efficacy and safety of fedratinib compared to best available therapy (BAT) in subjects with DIPSS (Dynamic International Prognostic Scoring System)-intermediate or high-risk primary myelofibrosis (PMF), post-polycythemia vera myelofibrosis (post-PV MF), or post-essential thrombocythemia myelofibrosis (post-ET MF) and previously treated with ruxolitinib. The primary objective of the study is to evaluate the percentage of subjects with at least 35% spleen volume reduction in the fedratinib and the BAT arms.
|
This Phase 3, multicenter, randomized, two-arm, open-label study will include subjects with intermediate or high-risk (as per the DIPSS score) primary myelofibrosis (PMF), postpolycythemia vera myelofibrosis (post-PV MF), or post-essential thrombocythemia myelofibrosis (post-ET MF). This study will be conducted in compliance with International Council for Harmonisation (ICH) Good Clinical Practices (GCPs).
Study design includes:
|
Interventional
|
Phase 3
|
Allocation: Randomized Intervention Model: Parallel Assignment Masking: None (Open Label) Primary Purpose: Treatment
|
- Primary Myelofibrosis
- Post-Polycythemia Vera
- Myelofibrosis
|
|
- Experimental: Fedratinib 400mg/day
Will include up to 128 subjects receiving fedratinib 400 mg self-administered Investigational Product (IP) on an outpatient basis, once daily preferably together with food during an evening meal at the same time each day in consecutive 4-week (28-day) cycles.
Intervention: Drug: FEDRATINIB
- Active Comparator: Best Available Therapy (BAT)
Best-available Investigator-selected therapy included a number of available compounds to treat MF and/or its symptoms and was chosen by the investigator for each subject. Therapy changed at different times during the treatment period. No investigational agents (e.g. not approved for the treatment of any indication) were allowed. BAT also included the choice of no treatment.
Intervention: Drug: Best Available Therapy (BAT)
|
Not Provided
|
|
Recruiting
|
192
|
Same as current
|
August 24, 2024
|
February 24, 2022 (Final data collection date for primary outcome measure)
|
Inclusion Criteria:
- Subject is at least 18 years of age at the time of signing the informed consent form (ICF)
- Subject has an Eastern Cooperative Oncology Group (ECOG) Performance Score (PS) of 0, 1 or 2
- Subject has diagnosis of primary myelofibrosis (PMF) according to the 2016 World Health Organization (WHO) criteria, or diagnosis of post-ET or post-PV myelofibrosis according to the IWG-MRT 2007 criteria, confirmed by the most recent local pathology report
- Subject has a DIPSS Risk score of Intermediate-2 or High
- Subject has a measurable splenomegaly during the screening period as demonstrated by spleen volume of ≥ 450 cm3 by MRI or CT-scan and by palpable spleen measuring ≥ 5 cm below the left costal margin
- Subject has a measurable total symptoms score (≥ 1) as measured by the Myelofibrosis Symptom Assessment Form (MFSAF)
-
Subject has been previously exposed to ruxolitinib, and must meet at least one of the following criteria (a and/or b)
- Treatment with ruxolitinib for ≥ 3 months with inadequate efficacy response (refractory) defined as < 10% spleen volume reduction by MRI or < 30% decrease from baseline in spleen size by palpation or regrowth (relapsed) to these parameters following an initial response
-
Treatment with ruxolitinib for ≥ 28 days complicated by any of the following (intolerant):
- Development of a red blood cell transfusion requirement (at least 2 units/month for 2 months) or
- Grade ≥ 3 AEs of thrombocytopenia, anemia, hematoma, and/or hemorrhage while on treatment with ruxolitinib
- Subject must have treatment-related toxicities from prior therapy resolved to Grade 1 or pretreatment baseline before start of last therapy prior to randomization
- Subject must understand and voluntarily sign an ICF prior to any study-related assessments/procedures being conducted
- Subject is willing and able to adhere to the study visit schedule and other protocol requirements
-
A female of childbearing potential (FCBP) must:
- Have 2 negative pregnancy tests as verified by the Investigator during screening prior to starting study treatment. She must agree to ongoing pregnancy testing during the course of the study, and after end of study treatment. This applies even if the subject practices true abstinence from heterosexual contact.
- Either commit to true abstinence from heterosexual contact (which must be reviewed on a monthly basis and source documented) or agree to use and be able to comply with highly effective contraception without interruption, -14 days prior to starting investigational product, during the study treatment (including dose interruptions), and for 30 days after discontinuation of study treatment.
Note: A female of childbearing potential (FCBP) is a female who: 1) has achieved menarche at some point, 2) has not undergone a hysterectomy or bilateral oophorectomy, or 3) has not been naturally postmenopausal (amenorrhea following cancer therapy does not rule out childbearing potential) for at least 24 consecutive months (ie, has had menses at any time in the preceding 24 consecutive months).
- A male subject must:
Practice true abstinence (which must be reviewed on a monthly basis) or agree to use a condom during sexual contact with a pregnant female or a female of childbearing potential while participating in the study, during dose interruptions and for at least 30 days following investigational product discontinuation, or longer if required for each compound and/or by local regulations, even if he has undergone a successful vasectomy
Exclusion Criteria:
-
Any of the following laboratory abnormalities:
- Platelets < 50 x 109/L
- Absolute neutrophil count (ANC) < 1.0 x 109/L
- White blood count (WBC) > 100 x 109/L
- Myeloblasts ≥ 5 % in peripheral blood
- Estimated glomerular filtration rate < 30 mL/min/1.73 m2 (as per the Modification of Diet in Renal Disease [MDRD] formula)
- Serum amylase or lipase > 1.5 x upper limit of normal (ULN)
- Aspartate aminotransferase (AST) or alanine aminotransferase (ALT) > 3 x upper limit of normal (ULN)
- Total bilirubin > 1.5 x ULN, subject's total bilirubin between 1.5 - 3.0 x ULN are eligible if the direct bilirubin fraction is < 25% of the total bilirubin
- Subject is pregnant or lactating female
- Subject with previous splenectomy
- Subject with previous or planned hematopoietic cell transplant
- Subject with prior history of encephalopathy, including Wernicke's (WE)
- Subject with signs or symptoms of encephalopathy, including WE (eg, severe ataxia, ocular paralysis or cerebellar signs)
- Subject with thiamine deficiency, defined as thiamine levels in whole blood below normal range according to the central laboratory and not demonstrated to be corrected prior to randomization
- Subject with concomitant treatment with or use of pharmaceutical, herbal agents or food known to be strong or moderate inducers of Cytochrome P450 3A4 (CYP3A4), or dual CYP2C19 and CYP3A4 inhibitors
- Subject on any chemotherapy, immunomodulatory drug therapy (eg, thalidomide, interferon-alpha), anagrelide, immunosuppressive therapy, systemic corticosteroids > 10 mg/day prednisone or equivalent. Subjects who have had prior exposure to hydroxyurea (eg, Hydrea) in the past may be enrolled into the study as long as it has not been administered within 14 days prior to randomization
- Subject has received ruxolitinib within 14 days prior to randomization
- Subject with previous exposure to Janus kinase (JAK) inhibitor(s) other than ruxolitinib treatment
- Subject on treatment with aspirin with doses > 150 mg daily
- Subject with major surgery within 28 days prior to randomization
- Subject with diagnosis of chronic liver disease (eg, chronic alcoholic liver disease, autoimmune hepatitis, sclerosing cholangitis, primary biliary cirrhosis, hemochromatosis, non-alcoholic steatohepatitis)
- Subject with prior malignancy other than the disease under study unless the subject has not required treatment for the malignancy for at least 3 years prior to randomization. However, subject with the following history/concurrent conditions provided successfully treated may enroll: non-invasive skin cancer, in situ cervical cancer, carcinoma in situ of the breast, incidental histologic finding of prostate cancer (T1a or T1b using the tumor, nodes, metastasis [TNM] clinical staging system), or is free of disease and on hormonal treatment only
- Subject with uncontrolled congestive heart failure (New York Heart Association Classification 3 or 4)
- Subject with known human immunodeficiency virus (HIV), known active infectious Hepatitis B (HepB), and/or known active infectious Hepatitis C (HepC)
- Subject with serious active infection
- Subject with presence of any significant gastric or other disorder that would inhibit absorption of oral medication
- Subject is unable to swallow capsule
- Subject with any significant medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from participating in the study
- Subject has any condition including the presence of laboratory abnormalities, which places the subject at unacceptable risk if he/she were to participate in the study
- Subject has any condition that confounds the ability to interpret data from the study
- Subject with participation in any study of an investigational agent (drug, biologic, device) within 30 days prior to randomization
- Subject with a life expectancy of less than 6 months
|
Sexes Eligible for Study: |
All |
|
18 Years and older (Adult, Older Adult)
|
No
|
Contact: Associate Director Clinical Trial Disclosure |
1-888-260-1599 |
clinicaltrialdisclosure@celgene.com |
|
|
Australia, Austria, Belgium, China, Czechia, France, Germany, Hungary, Ireland, Italy, Korea, Republic of, Netherlands, Poland, Russian Federation, Spain, United Kingdom
|
|
|
NCT03952039
|
FEDR-MF-002 U1111-1223-2962 ( Registry Identifier: WHO ) 2018-003411-21 ( EudraCT Number )
|
No
|
Studies a U.S. FDA-regulated Drug Product: |
Yes |
Studies a U.S. FDA-regulated Device Product: |
No |
|
Plan to Share IPD: |
Yes |
Plan Description: |
Information relating to our policy on data sharing and the process for requesting data can be found at the following link:
https://www.celgene.com/research-development/clinical-trials/clinical-trials-data-sharing/
|
Supporting Materials: |
Study Protocol |
Supporting Materials: |
Statistical Analysis Plan (SAP) |
Supporting Materials: |
Informed Consent Form (ICF) |
Supporting Materials: |
Clinical Study Report (CSR) |
Supporting Materials: |
Analytic Code |
Time Frame: |
See Plan Description |
Access Criteria: |
See Plan Description |
URL: |
https://www.celgene.com/research-development/clinical-trials/clinical-trials-data-sharing/ |
|
Celgene
|
Celgene
|
Impact Biomedicines, Inc., a wholly owned subsidiary of Celgene Corporation
|
Study Director: |
Vishwanath Gharpure, MD |
Celgene Corporation |
|
Celgene
|
March 2021
|
|