Safety and Tolerability of StroMel™ in Subjects with Moderate to Severe Osteoarthritis of the Knee Joint

Akan Biosciences

Status and phase

Not yet enrolling

Phase 2

Phase 1

Conditions

Osteo Arthritis Knee

Treatments

Biological: StroMel

Study type

Interventional

Funder types

Industry

Identifiers

NCT04750252

StroMel-01

Details and patient eligibility

About

The aim of this trial is to evaluate the safety and tolerability of autologous StroMel™ for the treatment of moderate to severe OA of the knee joint.

Enrollment

20 estimated patients

Sex

All

Ages

25 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Adults between the ages of 25-65 years
Body Mass Index (BMI) less than 40 kg/m2
Ambulatory and in good general health as described by vital signs (blood pressure 90/60 mm Hg to 120/80 mm Hg, pulse rate 60-100 beats per minute, temperature 97.2-99.1 °F) and normal blood chemistry.
Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) Pain score of ≥ 11 (worst possible = 20) over the previous 7 days
OA of the knee with Kellgren and Lawrence radiographic classification (Grade 2-4 inclusive) within the last 6 months
Minimum score of 40 out of possible 100 on the VAS (Visual Analog Scale) for pain.
Patients who have failed to adequately respond for at least 6 months to at least 2 OA therapies that include conservative, non-pharmacological therapy and simple analgesics (e.g., acetaminophen); nonsteroidal anti-inflammatory drugs (NSAIDS); avoidance of activities that cause joint pain; exercise; weight loss; physical therapy; and removal of excess fluid from the knee.
Have suitable knee joint anatomy for intra-articular injection.
For adults of reproductive potential: use of effective contraception for at least 1 month prior to screening and agreement to use such a method during study participation.

Exclusion criteria

Reactive arthritis, rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, or arthritis associated with inflammatory bowel disease.
Subject with an infection that requires parenteral antibiotic administration.
Active infection or crystal disease in the index joint within 1 month of screening
History of fracture in the index limb, joint instability, or history of acute dislocation within 12 months of screening, or fracture with sequelae at any time
Intra-articular treatment of any joint with any of the following agents within 6 months of screening: Any corticosteroid preparation (investigational or marketed), sodium hyaluronate, any biologic agent (e.g., platelet rich plasma (PRP) injection, stem cells, prolotherapy, amniotic fluid injection); investigational six months prior to enrollment.
Presence of surgical hardware or other foreign body in the index joint
Subjects who were administered with immunosuppressants such as cyclosporin A or azathioprine within 6 weeks before screening.
Planned or anticipated surgery of the joint during the study period
Allergies to anesthesia
Subjects who tested positive for HIV, HCV, WNV, CMV, HBV, HTLV, ZIKA, syphilis, flu or COVID-19. Note: CMV is not a relevant communicable disease agent. A subject who tests positive or reactive for CMV is not necessarily ineligible. Physicians will determine donor eligibility for subjects with positive CMV test results.
History of lipid disorders: lipedema, lipomatosis, or lipodystrophies.
Active cancer, chemotherapy, or other malignancies in the last 6 months.
Recent history of DVT or pulmonary embolism requiring anticoagulants or other medicines per the hematologist.
Subject who participated in another clinical trial within 3 months before the screening visit
Any illness which, in the Investigator's judgment, will interfere with the subject's ability to comply with the protocol, compromise patient safety, or interfere with the interpretation of the study results.
Subjects who are breastfeeding
Subjects with uncontrolled arrhythmias
Subjects with hemophilia; factor II, V, VII, X, or XII deficiencies; or Von Willebrand's disease.