Status:

TERMINATED

Study of Human Placenta-derived Cells (PDA001) to Evaluate the Safety and Effectiveness for Patients With Active Rheumatoid Arthritis

Lead Sponsor:

Celularity Incorporated

Collaborating Sponsors:

Celgene Corporation

Conditions:

Rheumatoid Arthritis

Eligibility:

All Genders

18-75 years

Phase:

PHASE2

Brief Summary

The primary objective of the study is to assess the safety and efficacy of 2 dose groups (PDA001 versus vehicle control) in subjects with active rheumatoid Arthritis. The secondary objectives of the s...

Eligibility Criteria

Inclusion

  • Inclusion Criteria:
  • Subjects must satisfy the following criteria to be enrolled in the study:
  • Diagnosis of RA as defined by the 1987-revised ACR criteria.
  • RA, characterized by at least 6 out of 66 swollen joints and 6 out of 68 tender joints at Screening and Baseline, and at least 2 of the following: a C reactive protein level (CRP), greater than the upper limit of normal (ULN) ³ 1 mg/dl, an erythrocyte sedimentation rate (ESR) of at least 28 mm per hour, or morning stiffness lasting longer than 45 minutes.
  • Non responsive or intolerant to a minimum of 2 RA therapies which are classified as DMARDs, biologics, or corticosteroids.
  • Biological medication must be discontinued 30 day prior to the first dose of study drug, except golimumab and actemra which are 60 days, and infliximab, alefacept and efalizumab, which must have been discontinued 90 days prior to the first dose of IP.
  • Cytotoxic agents, including but not limited to chlorambucil, cyclophosphamide, nitrogen mustard, or other alkylating agents must have been discontinued 90 days prior to the first dose of IP.
  • Subjects must be able to tolerate intravenous infusions in both arms.
  • There should be no change in RA medication dose anticipated during the initial treatment and re treatment periods and the respective 12 week follow-up period for each dosing treatment period. The following rules apply for anti-rheumatic medications taken during the study:
  • DMARDs must have must have been stable for least 90 days prior to dosing with IP.
  • Low -dose corticosteroids are permitted (prednisolone ≤ 10 mg per day or equivalent). Corticosteroids must have been stable for at least 30 days prior to dosing with IP.
  • DMARDs and corticosteroids must remain stable throughout the initial 3 months of study and throughout subsequent treatment periods
  • The presence of any of the following will exclude a subject from enrollment:
  • Prior use of rituximab and other B-cell depleting therapies, abatacept, prior use of more than 2 biologic therapies.
  • Subject has received an investigational agent in any indication-within 60 days (or 5 half-lives, whichever is longer) prior to treatment with IP.
  • Subject has received previous cell therapy.
  • Serum creatinine concentration \> 2.0 mg/dl at screening.
  • Alkaline phosphatase \> 2.5x the upper limit of normal at screening.
  • Bilirubin level \> 1.5 mg/dL (unless subject has known Gilbert's disease).
  • Untreated chronic infection or treatment of any infection with antibiotics within 4 weeks prior to dosing with IP.
  • Positive HIV test at Screening. Positive Hepatitis B surface antigen at Screening. Positive Hepatitis C antibody at Screening.
  • Organic heart disease (e.g., congestive heart failure), myocardial infarction within six (6) months prior to screening or clinically significant findings on ECG at screening. Clinically significant arrhythmia.
  • Primary or secondary immunodeficiency.

Exclusion

    Key Trial Info

    Start Date :

    December 1 2010

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ACTUAL

    End Date :

    September 1 2013

    Estimated Enrollment :

    26 Patients enrolled

    Trial Details

    Trial ID

    NCT01261403

    Start Date

    December 1 2010

    End Date

    September 1 2013

    Last Update

    July 22 2020

    Active Locations (16)

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    Page 1 of 4 (16 locations)

    1

    Pinnacle Research Group

    Anniston, Alabama, United States, 36207

    2

    Advanced Pain Research Institute

    Arcadia, California, United States, 91007

    3

    UCLA

    Los Angeles, California, United States, 90095

    4

    Desert Medical Advances

    Palm Desert, California, United States, 92260