Sprifermin (AS902330) in Cartilage Injury Repair (CIR)

Merck KGaA (EMD Serono)

Status and phase: Terminated; Phase 2

Conditions: Isolated Cartilage Injury of the Knee

Treatments: Drug: Sprifermin (AS902330) 100 mcg; Drug: Sprifermin (AS902330) 30 mcg; Other: Placebo; Drug: Sprifermin (AS902330) 10 mcg

Study type: Interventional

Funder types: Industry

Identifiers

NCT01066871

EMR700692_003

Details and patient eligibility

About

Several people all over the world suffer from cartilage injuries in the knee. Symptoms include pain, joint swelling, and loss of function. Without repair, cartilage injury may ultimately lead to osteoarthritis (OA). Natural healing is poor, and to date treatment is available only for deep cartilage defects involving also the underlying bone. A promising candidate for drug treatment of cartilage injury is sprifermin (AS902330), a recombinant form of the human fibroblast growth factor (FGF) 18.

So far, the drug has been used in subjects with different stages of knee OA in two ongoing studies without emerging safety issues following single and multiple intra-articular injections of ascending doses. However, OA represents late-stage cartilage injury, where repair might be difficult due to diffuse damage, reduced responsiveness of the cartilage, and/or the involvement of other joint structures.

This clinical trial is meant to provide the proof of concept and to identify an efficacious dose of sprifermin (AS902330) for the treatment of adult subjects with acute cartilage injuries of the knee. The first subject for this trial was treated on the 19th of April 2010.

Enrollment: 74 patients

Sex: All

Ages: 18 to 45 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Acute cartilage lesion of ICRS grade 2 to 4 at the femoral condyle of the knee (= target knee)
• Age: 18 to 45 years
• Sex: male or female. Women of childbearing potential (that is, all female subjects after puberty unless they are post-menopausal for at least 2 years or surgically sterile) must have negative serum and urine pregnancy tests at screening and Visit 1, respectively, and must use a highly effective method of contraception.
• History of pain and effusion of the target knee post-injury
• Injury within 4 to 12 weeks prior to 1st treatment with investigational medicinal product (IMP)
• Written informed consent prior to any trial-related activity

Exclusion criteria

• Personal medical history of osteoarthritis OA in either knee
• Any previous surgery on the target knee
• History of swelling of the target knee along with pain on weight-bearing, or arthroscopy for diagnostic purposes during the 12 months preceding injury
• Corticosteroid (intra-articular) injection into the target knee during the preceding 12 months
• Any other intra-articular injection into the target knee during the preceding 3 months
• Any concurrent injury (for example, arthrolith, anterior cruciate ligament rupture, meniscus tear) of the target knee requiring surgical intervention
• OA or any pre-existing cartilage damage in the target knee, as revealed by MRI
• Legal incapacity or limited legal capacity
• Subjects who are imprisoned or institutionalized by regulatory or court order
• Pregnancy or lactation
• Participation in another clinical trial within the past 30 days
• Any condition or findings in the medical history or in the pre-trial assessments that in the opinion of the Investigator constitutes a risk or contraindication for participation in the trial or that could interfere with the trial objectives, conduct or evaluation
• Known hypersensitivity to the trial treatment or diluents
• Significant renal or hepatic impairment, as indicated by: Aspartate aminotransferase (AST), alanine aminotransferase (ALT), or alkaline phosphatase (ALP) greater than (>) 3 times the upper limit of normal (ULN); total bilirubin >1.5 times ULN (except in case of Gilbert's syndrome); creatinine >1.5 times ULN; hemoglobin less than (<5.5) millimole per liter (mmol/L), white blood cell count (WBC) <2.5 * 10^9 per liter, or platelets <75 *10^9 per liter)
• Any suspicion of intra-articular infection
• Any known active infections that may compromise the immune system such as human immunodeficiency virus (HIV), Hepatitis B or C infection
• History of sarcoma and/or of other active malignancy within five years, except adequately treated basal cell or squamous cell carcinoma of the skin
• Open growth plate, as revealed by MRI
• Diagnostic arthroscopy after injury and within 4 weeks prior to treatment start

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

---

74 participants in 4 patient groups, including a placebo group

Sprifermin (AS902330) 10 mcg

Experimental group

Treatment:

Drug: Sprifermin (AS902330) 10 mcg

Sprifermin (AS902330) 30 mcg

Experimental group

Treatment:

Drug: Sprifermin (AS902330) 30 mcg

Sprifermin (AS902330) 100 mcg

Experimental group

Treatment:

Drug: Sprifermin (AS902330) 100 mcg

Placebo

Placebo Comparator group

Treatment:

Other: Placebo