A Clinical Study to Test Efficacy and Safety of CNTX-4975-05 in Patients With Osteoarthritis Knee Pain



Status:Active, not recruiting
Conditions:Osteoarthritis (OA)
Therapuetic Areas:Rheumatology
Healthy:No
Age Range:40 - 95
Updated:12/9/2018
Start Date:January 24, 2018
End Date:February 29, 2020

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A Randomized, Double-blind, Placebo-controlled, Single Injection, 52-Week Study to Evaluate the Efficacy and Safety of an Intra-articular Injection of CNTX-4975-05 in Subjects With Chronic, Moderate-to-severe Osteoarthritis Knee Pain

This is a phase 3, randomized, double-blind, placebo-controlled, single injection, 52-week
study to evaluate the efficacy and safety of CNTX-4975-05 in subjects with chronic,
moderate-to-severe osteoarthritis knee pain.


Key Inclusion Criteria:

- Male or female subjects between 40 and 95 years of age (inclusive) at the time of the
Screening Visit with the ability to comply with answering the electronic diary using
the study-provided tablet computers.

- Confirmation of osteoarthritis (OA) of the knee.

- Confirmation of OA of the index knee.

- Moderate to severe pain in the index knee associated with OA must be stable for a
minimum of 6 months prior to Screening, as assessed by the investigator.

- BMI ≤45 kg/m^2.

- Must have failed 2 or more prior therapies.

- Females not of childbearing potential, defined as post-menopausal for at least 1 year,
or surgically sterile, or practicing one of the following medically acceptable methods
of birth control throughout the study period.

Key Exclusion Criteria:

- Joint replacement surgery of the index knee at any time, or open surgery of the index
knee in the past 24 months.

- Prior arthroscopic surgery of the index knee within 6 months of Screening.

- Any painful conditions of the index knee due to joint disease other than OA.

- Periarticular pain from any cause.

- Pain in the non-index knee that is >3 numeric pain rating scale (NPRS) (0-10) when
walking or at rest.

- Other chronic pain anywhere in the body that requires the use of analgesic
medications.

- Instability of the index knee.

- Misalignment (>10 degrees varus or valgus) of the index knee on standing.

- Documented history of neuropathic arthropathy or finding of bony fragmentation in the
index knee with imaging.

- Physical/ occupational/ chiropractic therapy for the lower extremities or acupuncture
for the lower extremities within 30 days of Screening, or need for such therapy during
the study.

- Plans to have surgery, other invasive procedures, or IA injections while participating
in the study.

- Has used topical capsaicin on the index knee within 90 days of Screening.

- Current use of opioids for any condition other than for OA of the index knee.

- Corticosteroid injection into the index knee within 90 days of Screening.

- Received IA viscosupplementation (eg, Synvisc®, Hyalgan®) within 90 days of Screening.
We found this trial at
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Birmingham, Alabama 35242
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860 Peachwood Drive
DeLand, Florida 32720
(386) 740-0770
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800 Washington St
Boston, Massachusetts 02111
(617) 636-5000
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400 Tower Rd Ne
Marietta, Georgia 30060
678-581-5252
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Anaheim, California 92801
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1635 North George Mason Drive
Arlington, Virginia 22205
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Austin, Texas 78745
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Birmingham, Alabama 35209
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Cerritos, California 90703
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Charlottesville, Virginia 22911
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Evansville, Indiana 47714
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La Mesa, California 91942
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Las Vegas, Nevada 89119
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286 Westward Drive
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Mobile, Alabama 36608
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465 South Washington Street
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North Hollywood, California 91606
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Tampa, Florida 33603
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Traverse City, Michigan 49684
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