Feasibility Study of Aastrom Tissue Repair Cells to Treat Non-Union Fractures.

Pseudarthrosis Clinical Trial

Official title:

TRC Autologous Bone Marrow Cells for the Treatment of Appendicular Skeletal Fracture Non-Union

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT00424567
• Other study ID #: ABI 55-0503-1
• Status: Terminated
• Phase: Phase 1/Phase 2
• Start date: October 2003
• Est. completion date: June 2007

Study information

• Verified date: May 2021
• Source: Vericel Corporation
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this multi-center study is to obtain clinical data to substantiate that Aastrom TRC autologous bone marrow cells will regenerate bone in patients with established (appendicular skeletal) non union fractures, when used with one of the commonly employed commercially available allograft chip matrices.

Description:

The current standard of care for regeneration of atrophic long bone fracture non-union is autologous bone and marrow chiseled from the patient's iliac crest in open surgery under general anesthesia. This method for harvesting bone and marrow is associated with substantial morbidity of long-term pain, the possibility of deep-seated infection at the site of the bone harvest and other indirect consequences such as extended time of surgery, substantial expense and the potential for blood transfusion. The procedure is also associated with a bone graft failure rate of at least 20%.

Due to the substantial morbidity resulting from the aggressive open surgical procedure, alternatives are sought. Current alternatives to autologous bone include commercially available synthetic, xenograft and allograft matrices, either used alone or combined with bone autograft. Cell-free substitutes, such as matrices combined with platelet rich plasma or recombinant bone morphogenic proteins for osteoinductivity, are also used. These alternatives, although less morbid than a full bone harvest, have not yet been stringently determined to be equivalent. Therefore, there is a continuing search for additional improved alternatives.

Aastrom Biosciences, Inc. has developed a unique process for growing human bone marrow, including the early stem cell populations, from small samples of percutaneously aspirated bone marrow. The process is carried out in the AastromReplicell Cell Production System (ARS).

The study will be performed to obtain clinical data to substantiate that Aastrom TRC autologous bone marrow cells will regenerate bone in patients with established non union fractures, when used with one of the commonly employed commercially available allograft chip matrices.

The bone marrow cells will be obtained by a brief, percutaneous, small volume aspiration (approximately 30 - 50 ml) from the posterior iliac crest obtained under local and conscious sedation. Percutaneous marrow aspiration is substantially less morbid and time consuming than the current open surgical process of bone autograft harvest.

The study will treat up to 36 patients (11 in the first group and 25 in a second group).

Patients will be treated using standard surgical procedures for the treatment of non union fractures (including commonly used hardware needed to stabilize the fracture). The processed cells will be mixed with commercially available bone matrix during surgery and placed in the area of the fracture.

Patients will be monitored for 12 months following the surgery.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 36
• Est. completion date: June 2007
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Type IIIA or IIIB fracture

• Fracture gap < 6 cm.

• Distance of > 4 cm from joint

• No clinical signs of infection at the wound site or fracture site.

• Adult patients >18 years of age.

• Male patients or female patients who are not pregnant or lactating.

• Patients must have normal organ and marrow function as defined below:

1. Leukocytes >=3000/microliters

2. Absolute neutrophil count >=1500/microliters

3. Platelets >=100,000/microliters

4. AST (SGOT)/ALT (SGPT) <2.5 x institutional limits

5. Creatinine within normal limits or creatinine clearance calculated)>=60 mL/min/1.73 square miter with creatinine above institutional normal.

• Patients able to give informed consent

Exclusion Criteria:

• Other long bone fractures, e.g clavicle

• Patients unable to discontinue ethanol use after surgery including those requiring pharmacologic adjuvant assistance.

1. Although not an exclusion criteria, the attending physician shall discuss with the patient the advantages of discontinuing smoking cigarettes and/or cigars during the term of the study including discontinuing the use of pharmacologic adjuvant assistance such as nicotine suppression.

2. The use or discontinuance of ethanol and/or cigarettes/cigars will be noted in the patient's case report forms.

• Patients who require corticosteroid anti-inflammatory therapy after surgery.

• Patients with genetic metabolic bone disease such as hypophosphatasia, or metabolic bone disorders such as primary or secondary hyperparathyroidism caused by chronic renal insufficiency or other disorders.

• Patients unable to tolerate general anesthesia defined as an ASA criteria of 0 or 1.

• Patients on systemic antibiotics for suspected wound or fracture site infection.

• Patients with diabetes.

• Glasgow score of < 13.

• Injury severity score of > 25.

• Allergy to protein products derived from mammalian sources (horse, bovine or porcine) required in the ex-vivo cell production process.

Related Conditions & MeSH terms

• Fracture, Ununited
• Fractures, Bone
• Fractures, Ununited
• Pseudarthrosis

Intervention

Procedure:
• Fracture surgery

Drug:
• Cultured Bone Marrow Tissue

Locations

Country	Name	City	State
United States	University of Michigan Medical School	Ann Arbor	Michigan
United States	Lutheran Medical Center	Brooklyn	New York
United States	Illinois Bone and Joint Institute	Des Plaines	Illinois
United States	William Beaumont Hospital	Royal Oak	Michigan

Sponsors (1)

Lead Sponsor	Collaborator
Vericel Corporation

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The primary endpoint will be the proportion of patients with demonstrated healing, including bone formation, at 12 months (or until completely healed) from surgery.