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Dose Escalation Study of UCART19 in Adult Patients With Relapsed / Refractory B-cell Acute Lymphoblastic Leukaemia (CALM)

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ClinicalTrials.gov Identifier: NCT02746952
Recruitment Status : Recruiting
First Posted : April 21, 2016
Last Update Posted : February 27, 2018
Sponsor:
Information provided by (Responsible Party):
Servier

Brief Summary:
The purpose of this study is to evaluate the safety and tolerability of ascending doses of UCART19 in patients with relapsed / refractory (R/R) B-cell acute lymphoblastic leukaemia (B-ALL) and to determine the maximum tolerated dose (MTD).

Condition or disease Intervention/treatment Phase
B-cell Acute Lymphoblastic Leukemia Genetic: UCART19 Phase 1

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 40 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Phase I, Open Label, Dose-escalation Study to Evaluate the Safety, Expansion and Persistence of a Single Dose of UCART19 (Allogeneic Engineered T-cells Expressing Anti-CD19 Chimeric Antigen Receptor), Administered Intravenously in Patients With Relapsed or Refractory CD19 Positive B-cell Acute Lymphoblastic Leukaemia (B-ALL)
Actual Study Start Date : August 1, 2016
Estimated Primary Completion Date : June 2018
Estimated Study Completion Date : June 2018


Arm Intervention/treatment
Experimental: UCART19 Genetic: UCART19
Other Name: S68587




Primary Outcome Measures :
  1. Dose Limiting Toxicities (DLTs) occurence [ Time Frame: Up to day 28 post UCART19 infusion ]

Secondary Outcome Measures :
  1. Incidence and Severity of Adverse Events as a Measure of Safety and Tolerability [ Time Frame: Through study completion, approximately 16 weeks ]
    Adverse events assessed according to NCI-CTCAE v4.03 criteria

  2. Objective Response Rate [ Time Frame: At day 28, at day 84 and overall ]
    Proportion of patients in whom a response among molecular remission, morphologic complete remission and complete remission with incomplete blood count recovery, as defined by standard disease-specific criteria, will be observed.

  3. Duration of response [ Time Frame: From the time that response criteria are first met until the date of progression or death (whatever the reason of death), whichever occurs first, assessed up to day 84 ]
  4. Time to response [ Time Frame: From the date of UCART19 administration until the date that response criteria are met, assessed up to day 84 ]
  5. Progression Free Survival (PFS) [ Time Frame: From the date of UCART19 administration until the date of progression or the date of death (whatever the reason of death), whichever occur first, assessed up to day 84 ]
  6. Disease-Specific Survival (DSS) [ Time Frame: From the date of UCART19 administration to the date of death due to the studied disease or to UCART19, assessed up to day 84 ]


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Ages Eligible for Study:   16 Years and older   (Child, Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Male or female participant
  • Age ≥ 16 years
  • Patient with relapsed or refractory CD19 positive B-acute lymphoblastic leukaemia (B-ALL)
  • Estimated life expectancy ≥ 12 weeks (according to investigator's judgement)
  • Eastern Cooperative Oncology Group (ECOG) performance status < 2

Exclusion Criteria:

  • Previous treatment with investigational gene or cell therapy medicine products
  • Use of investigational products or other anti-leukemic therapy within 5 half-lives or within 14 days prior to UCART19 administration whichever has a shorter duration
  • CD19 negative B-cell leukaemia
  • Burkitt cell or mixed lineage acute leukaemia

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02746952


Contacts

Locations
United States, Massachusetts
Massachusetts General Hospital Not yet recruiting
Boston, Massachusetts, United States, MA 02114
United States, Pennsylvania
Hospital of the University of Pennsylvania Not yet recruiting
Philadelphia, Pennsylvania, United States, 19104
United States, Texas
University of Texas MD Anderson Cancer Center Recruiting
Houston, Texas, United States, 77030
France
Hôpital Saint-Antoine Not yet recruiting
PARIS Cedex 12, France, 75571
Hôpital Saint-Louis Not yet recruiting
Paris, France, 75010
United Kingdom
King's College Hospital NHS Foundation Trust Recruiting
London, United Kingdom, SE5 9RS
Contact: Benjamin Reuben, MD, PhD         
Principal Investigator: Benjamin Reuben, MD, PhD         
The Christie NHS Foundation Trust Not yet recruiting
Manchester, United Kingdom, M20 4BX
Sponsors and Collaborators
Servier
Investigators
Principal Investigator: Reuben Benjamin, MD, PhD King's College Hospital NHS Trust

Additional Information:
Study Data/Documents: Individual Participant Data Set  This link exits the ClinicalTrials.gov site

Responsible Party: Servier
ClinicalTrials.gov Identifier: NCT02746952     History of Changes
Other Study ID Numbers: CL1-68587-002
2016-000296-24 ( EudraCT Number )
First Posted: April 21, 2016    Key Record Dates
Last Update Posted: February 27, 2018
Last Verified: February 2018
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Yes
Plan Description:

Researchers can ask for a study protocol, patient-level and/or study-level clinical trial data including clinical study reports (CSRs).

They can ask all interventional clinical studies:

  • submitted for new medicines and new indications approved after 1 January 2014 in the European Economic Area (EEA) or the United States (US).
  • Where Servier or an affiliate are the Marketing Authorization Holders (MAH). The date of the first Marketing Authorization of the new medicine (or the new indication) in one of the EEA Member States will be considered within this scope.
Supporting Materials: Study Protocol
Statistical Analysis Plan (SAP)
Informed Consent Form (ICF)
Clinical Study Report (CSR)
Time Frame: After Marketing Authorisation in EEA or US if the study is used for the approval.
Access Criteria: Researchers should register on Servier Data Portal and fill in the research proposal form. This form in four parts should be fully documented. The Research Proposal Form will not be reviewed until all mandatory fields are completed.
URL: http://clinicaltrials.servier.com

Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No

Additional relevant MeSH terms:
Epstein-Barr Virus Infections
Leukemia
Precursor Cell Lymphoblastic Leukemia-Lymphoma
Leukemia, Lymphoid
Burkitt Lymphoma
Neoplasms by Histologic Type
Neoplasms
Lymphoproliferative Disorders
Lymphatic Diseases
Immunoproliferative Disorders
Immune System Diseases
Herpesviridae Infections
DNA Virus Infections
Virus Diseases
Tumor Virus Infections
Lymphoma, B-Cell
Lymphoma, Non-Hodgkin
Lymphoma