Trial Review

The ANZCTR website will be unavailable from 1pm until 3pm (AEDT) on Wednesday the 30th of October for website maintenance. Please be sure to log out of the system in order to avoid any loss of data.

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been endorsed by the ANZCTR. Before participating in a study, talk to your health care provider and refer to this information for consumers
Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT02445222




Registration number
NCT02445222
Ethics application status
Date submitted
1/05/2015
Date registered
15/05/2015
Date last updated
26/07/2024

Titles & IDs
Public title
CAR-T Long Term Follow Up (LTFU) Study
Scientific title
Long Term Follow-Up of Patients Exposed to Lentiviral-Based CAR T-Cell Therapy
Secondary ID [1] 0 0
2014-001673-14
Secondary ID [2] 0 0
CCTL019A2205B
Universal Trial Number (UTN)
Trial acronym
PAVO
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Long Term Safety of Patients Receiving CAR-T in an Eligible Clinical Trial or Managed Access Program 0 0
Condition category
Condition code

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Other - Previously treated CAR-T patients

Other: Previously treated CAR-T patients - Patients who previously were exposed to lentiviral-based CART cell therapy


Treatment: Other: Previously treated CAR-T patients
Lentiviral-based CAR-T cell therapy
Intervention code [1] 0 0
Treatment: Other
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Percentage of patients with certain events (see description)
Timepoint [1] 0 0
at M3 post treatment, M6, M9, M12 and then, every 6M up to year 5, yearly until year 15.
Secondary outcome [1] 0 0
Percentage of patients with detectable CAR transgene levels in peripheral blood by q-PCR at pre- specified time points
Timepoint [1] 0 0
at M3 post treatment, M6, M9, M12 and every 6M up to year 5, yearly until year 15.
Secondary outcome [2] 0 0
Percentage of patients with detectable RCL by VSV-G
Timepoint [2] 0 0
at M3 post treatment then M6, M9, M12 and every 6M up to year 5, yearly until year 15
Secondary outcome [3] 0 0
Percentage of patients who relapse or progress among patients who had not relapsed or progressed at study entry/re-entry;Incidence of death
Timepoint [3] 0 0
at M3 post treatment then M6, M9, M12 and every 6M up to year 5, yearly until year 15.
Secondary outcome [4] 0 0
B- and T- lymphocyte count
Timepoint [4] 0 0
at M3 post treatment then M6, M9, M12 and every 6M up to year 5, yearly until year 15.
Secondary outcome [5] 0 0
Height and weight, Tanner staging, menstruation status
Timepoint [5] 0 0
at M3 post treatment then M6, M12 and every year until year 15.

Eligibility
Key inclusion criteria
* All patients who have received a CAR-T therapy and completed or discontinued early from a Novartis sponsored treatment protocol that utilized CAR-T cells or from any CAR-T trial sponsored by the University of Pennsylvania with which Novartis has a contractual agreement to co-develop the CAR technology.
* Patients who have provided informed consent for the long term follow up study prior to their study participation .
Minimum age
No limit
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
* There are no specific exclusion criteria for this study.

Study design
Purpose of the study
Other
Allocation to intervention
NA
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Single group
Other design features
Phase
Phase 3
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Recruiting
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
5/01/2016
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
22/02/2036
Actual
Sample size
Target
1400
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
VIC
Recruitment hospital [1] 0 0
Novartis Investigative Site - Melbourne
Recruitment hospital [2] 0 0
Novartis Investigative Site - Parkville
Recruitment hospital [3] 0 0
Novartis Investigative Site - Camperdown
Recruitment postcode(s) [1] 0 0
3000 - Melbourne
Recruitment postcode(s) [2] 0 0
3052 - Parkville
Recruitment postcode(s) [3] 0 0
NSW - Camperdown
Recruitment outside Australia
Country [1] 0 0
United States of America
State/province [1] 0 0
Arizona
Country [2] 0 0
United States of America
State/province [2] 0 0
California
Country [3] 0 0
United States of America
State/province [3] 0 0
Georgia
Country [4] 0 0
United States of America
State/province [4] 0 0
Illinois
Country [5] 0 0
United States of America
State/province [5] 0 0
Kansas
Country [6] 0 0
United States of America
State/province [6] 0 0
Massachusetts
Country [7] 0 0
United States of America
State/province [7] 0 0
Michigan
Country [8] 0 0
United States of America
State/province [8] 0 0
Minnesota
Country [9] 0 0
United States of America
State/province [9] 0 0
Missouri
Country [10] 0 0
United States of America
State/province [10] 0 0
New York
Country [11] 0 0
United States of America
State/province [11] 0 0
North Carolina
Country [12] 0 0
United States of America
State/province [12] 0 0
Ohio
Country [13] 0 0
United States of America
State/province [13] 0 0
Oregon
Country [14] 0 0
United States of America
State/province [14] 0 0
Pennsylvania
Country [15] 0 0
United States of America
State/province [15] 0 0
Texas
Country [16] 0 0
United States of America
State/province [16] 0 0
Utah
Country [17] 0 0
United States of America
State/province [17] 0 0
Wisconsin
Country [18] 0 0
Austria
State/province [18] 0 0
Linz
Country [19] 0 0
Austria
State/province [19] 0 0
Vienna
Country [20] 0 0
Austria
State/province [20] 0 0
Wien
Country [21] 0 0
Belgium
State/province [21] 0 0
Gent
Country [22] 0 0
Canada
State/province [22] 0 0
Ontario
Country [23] 0 0
Canada
State/province [23] 0 0
Quebec
Country [24] 0 0
Denmark
State/province [24] 0 0
Copenhagen
Country [25] 0 0
Finland
State/province [25] 0 0
Helsinki
Country [26] 0 0
France
State/province [26] 0 0
Paris 10
Country [27] 0 0
France
State/province [27] 0 0
Paris
Country [28] 0 0
France
State/province [28] 0 0
Pierre Benite
Country [29] 0 0
Germany
State/province [29] 0 0
Bavaria
Country [30] 0 0
Germany
State/province [30] 0 0
Berlin
Country [31] 0 0
Germany
State/province [31] 0 0
Frankfurt
Country [32] 0 0
Germany
State/province [32] 0 0
Hamburg
Country [33] 0 0
Germany
State/province [33] 0 0
Koeln
Country [34] 0 0
Germany
State/province [34] 0 0
Leipzig
Country [35] 0 0
Germany
State/province [35] 0 0
Muenchen
Country [36] 0 0
Germany
State/province [36] 0 0
Ulm
Country [37] 0 0
Germany
State/province [37] 0 0
Wuerzburg
Country [38] 0 0
Israel
State/province [38] 0 0
Ramat Gan
Country [39] 0 0
Israel
State/province [39] 0 0
Tel Aviv
Country [40] 0 0
Italy
State/province [40] 0 0
MB
Country [41] 0 0
Italy
State/province [41] 0 0
RM
Country [42] 0 0
Japan
State/province [42] 0 0
Fukuoka
Country [43] 0 0
Japan
State/province [43] 0 0
Hokkaido
Country [44] 0 0
Japan
State/province [44] 0 0
Miyagi
Country [45] 0 0
Japan
State/province [45] 0 0
Tokyo
Country [46] 0 0
Japan
State/province [46] 0 0
Kyoto
Country [47] 0 0
Netherlands
State/province [47] 0 0
CS
Country [48] 0 0
Netherlands
State/province [48] 0 0
Amsterdam
Country [49] 0 0
Netherlands
State/province [49] 0 0
Utrecht
Country [50] 0 0
Norway
State/province [50] 0 0
Oslo
Country [51] 0 0
Singapore
State/province [51] 0 0
Singapore
Country [52] 0 0
Spain
State/province [52] 0 0
Andalucia
Country [53] 0 0
Spain
State/province [53] 0 0
Barcelona
Country [54] 0 0
Spain
State/province [54] 0 0
Castilla Y Leon
Country [55] 0 0
Spain
State/province [55] 0 0
Catalunya
Country [56] 0 0
Spain
State/province [56] 0 0
Comunidad Valenciana
Country [57] 0 0
Spain
State/province [57] 0 0
Madrid
Country [58] 0 0
Taiwan
State/province [58] 0 0
Taipei
Country [59] 0 0
United Kingdom
State/province [59] 0 0
London

Funding & Sponsors
Primary sponsor type
Commercial sector/industry
Name
Novartis Pharmaceuticals
Address
Country
Other collaborator category [1] 0 0
Other
Name [1] 0 0
University of Pennsylvania
Address [1] 0 0
Country [1] 0 0

Ethics approval
Ethics application status

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Novartis Pharmaceuticals
Address 0 0
Novartis Pharmaceuticals
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Novartis Pharmaceuticals
Address 0 0
Country 0 0
Phone 0 0
1-888-669-6682
Fax 0 0
Email 0 0
Contact person for scientific queries

No information has been provided regarding IPD availability


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

No documents have been uploaded by study researchers.

Results not provided in https://clinicaltrials.gov/study/NCT02445222