Study on Autologous Osteoblastic Cells Implantation in Hypotrophic Non-Union Fractures

Bone Therapeutics

Status and phase: Terminated; Phase 3; Phase 2

Conditions: Long Bone Non-Union

Treatments: Drug: PREOB® Implantation; Procedure: Bone Autograft

Study type: Interventional

Funder types: Industry

Identifiers

NCT01756326

PREOB-NU3

Details and patient eligibility

About

Fracture healing is a complex physiological process caused by interaction of cellular elements, cytokines and signaling proteins, which results in the formation of new bone (Gerstenfeld et al., 2003). Depending on fracture site, complexity, co-morbidities and other factors, 10% of all fractures will eventually fail to unite.

Non-union fractures are defined as fractures that are at least six to nine months old and in which there have been no signs of healing for the last three months. Various causes have been evoked for impaired healing in hypotrophic (atrophic and oligotrophic) non-unions, including poor fracture stabilization, local infection and failure of the osteoblastic cells to multiply. Currently the treatment of choice for non-unions, particularly atrophic non-unions, is bone autograft (or allograft), combined or not with intramedullary nailing, plating, and external fixation devices (Kanakaris et al., 2007). This procedure produces good results but requires an invasive surgery of several hours under general anesthesia and a few days of hospitalization. Because of this, major complications have been reported in up to 20-30% of patients (Pieske et al., 2009, Zimmerman et al., 2009).

This Phase 2b/3 study aims at demonstrating the safety and efficacy of PREOB®, a proprietary population of autologous osteoblastic cells, in the treatment of hypotrophic non-union fractures of long bones. PREOB® will be compared to Bone Autograft in a non-inferiority design.

Enrollment: 5 patients

Sex: All

Ages: 18 to 65 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Ability to provide a written, dated, and signed informed consent prior to any study related procedure, and to understand and comply with study requirements
• Diagnosis of a non-infected hypotrophic non-union fracture of a long bone of at least 6 months at the time of treatment
• Normal hematology function

Exclusion criteria

• Positive serology for HIV, hepatitis B, hepatitis C, syphilis, HTLV-1
• Presence or previous history, or risk factors for diseases caused by prions
• Renal impairment, hepatic impairment
• Patient with poorly controlled diabetes mellitus, severe arterial diseases and/or neuropathy
• Insufficient fracture stability
• Recent osteosynthesis material or bone graft
• Multifocal fracture/non-unions

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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5 participants in 2 patient groups

PREOB® Implantation

Experimental group

Description:

Each patient will undergo a single administration of PREOB® into the non-union site, under local or loco-regional anesthesia.

Treatment:

Drug: PREOB® Implantation

Bone Autograft

Active Comparator group

Description:

Each patient will be treated by Bone Autograft according to standard-of-care procedure of the investigating site.

Treatment:

Procedure: Bone Autograft