AP-003-C Study to Confirm the Efficacy of Ampion™ in Adults With Pain Due to Severe Osteoarthritis of the Knee

Knee Osteoarthritis Clinical Trial

Official title:

A Phase 3 Randomized Study to Confirm the Efficacy of an Intra-Articular Injection of Ampion™ in Adults With Pain Due to Severe Osteoarthritis of the Knee

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03182686
• Other study ID #: AP-003-C
• Status: Completed
• Phase: Phase 3
• Start date: June 19, 2017
• Est. completion date: December 7, 2017

Study information

• Verified date: August 2022
• Source: Ampio Pharmaceuticals. Inc.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a phase 3 randomized study to confirm the efficacy of an intra-articular injection of Ampion™ in adults with pain due to severe osteoarthritis of the knee.

Description:

A Randomized Study to Confirm the Efficacy of an Intra-Articular Injection of Ampion™ in Adults With Pain Due to Severe Osteoarthritis of the Knee There will be a 7-day screening period for each subject followed by a 12-week participation period. The primary trial objective is to evaluate the clinical efficacy of Ampion using the Outcome Measures in Rheumatology Clinical Trials and Osteoarthritis Research Society International (OMERACT-OARSI) (using the Western Ontario and McMaster Universities Arthritis Index (WOMAC) 3.1 Index and Patient's Global Assessment as assessments). The secondary trial objectives are to evaluate the safety of a single intra-articular injection (4 mL) of Ampion.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 168
• Est. completion date: December 7, 2017
• Est. primary completion date: December 7, 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 40 Years to 85 Years

Eligibility

Inclusion Criteria:

• Able to provide written informed consent to participate in the study;
• Willing and able to comply with all study requirements and instructions of the site study staff;
• Must be ambulatory;
• Study knee must have a clinical diagnosis of osteoarthritis (OA) supported by radiological evidence (Kellgren Lawrence Grade IV) which is assessed locally (x-rays within the past 6 months of screening are acceptable);
• Moderate to moderately-severe OA pain in the study knee (rating of at least 1.5 on the WOMAC A, 5-point Likert Pain Subscale);
• Moderate to moderately-severe OA function in the study knee (rating of at least 1.5 on the WOMAC C, 5-point Likert Function Subscale);
• WOMAC A, 5-point Likert pain subscale <1.5 in the contralateral knee;
• Ability to discontinue non-steroidal anti-inflammatory drug (NSAID) use at Screening visit and/or 72 hours prior to the Baseline visit and for the duration of the clinical study (low-dose aspirin (81 mg) is allowed during the study);
• No analgesia (including acetaminophen) taken 24 hours prior to an efficacy measure;
• No known clinically significant liver abnormality (e.g. cirrhosis, transplant, etc.).

Exclusion Criteria:

• As a result of medical review and screening investigation, the Principal Investigator considers the subject unfit for the study
• A history of allergic reactions to human albumin (reaction to non-human albumin such as egg albumin is not an exclusion criterion)
• A history of allergic reactions to excipients in 5% human albumin (N-acetyltryptophan, sodium caprylate)
• Presence of tense effusions
• Inflammatory or crystal arthropathies, acute fractures, history of aseptic necrosis or joint replacement in the affected knee, as assessed locally by the Principal Investigator
• Isolated patella femoral syndrome, also known as chondromalacia
• Any other disease or condition interfering with the free use and evaluation of the study knee for the duration of the trial (e.g. cancer, congenital defects, spine osteoarthritis)
• Major injury to the study knee within the 12 months prior to screening
• Severe hip osteoarthritis ipsilateral to the study knee
• Any pain that could interfere with the assessment of study knee pain (e.g. pain in any other part of the lower extremities, pain radiating to the knee)
• Any pharmacological or non-pharmacological treatment targeting OA started or changed during the 4 weeks prior to randomization or likely to be changed during the duration of the study
• Pregnancy or planning to become pregnant during the study
• Use of the following medications:

1. No intra-articular (IA) injected medications in the study knee during the study (or 12 weeks prior to Baseline).

2. No analgesics containing opioids.

3. NSAIDs are not permitted during the study; acetaminophen is available as a rescue medication during the study from the provided supply.

4. No topical treatment on the study knee during the study

5. No significant anticoagulant therapy (e.g. Heparin or Lovenox) during the study (treatment such as low-dose Aspirin (81 mg) and Plavix are allowed)

6. No systemic treatments that may interfere with safety or efficacy assessments during the study

7. No immunosuppressants

8. No use of systemic or intra-articular corticosteroids

• No human albumin treatment in the 3 months before randomization or throughout the duration of the study

Related Conditions & MeSH terms

• Knee Arthritis
• Knee Osteoarthritis
• Knee Pain Chronic
• Osteoarthritis
• Osteoarthritis, Knee

Intervention

Biological:
• 4 mL injection of Ampion
4 mL injection of Ampion

Drug:
• 4 mL Injection of Placebo
4 mL Injection of Placebo

Locations

Country	Name	City	State
United States	Tekton Research	Austin	Texas
United States	Northwest Clinical Research Center	Bellevue	Washington
United States	Central Research Associates, Inc.	Birmingham	Alabama
United States	Healthcare Research Netword	Blue Island	Illinois
United States	CORE Orthopaedic Medical Center	Encinitas	California
United States	Arthritis Treatment Center	Frederick	Maryland
United States	St. Joseph Heritage	Fullerton	California
United States	Healthcare Network Research	Hazelwood	Missouri
United States	Drug Studies America	Marietta	Georgia
United States	Coastal Carolina Center at Lowcountry Orthopaedics	North Charleston	South Carolina
United States	Artemis Institute for Clinical Research	San Diego	California
United States	Westlake Medical Research	Thousand Oaks	California
United States	Heartland Research Associates	Wichita	Kansas

Sponsors (1)

Lead Sponsor	Collaborator
Ampio Pharmaceuticals. Inc.

Country where clinical trial is conducted

United States, 

References & Publications (1)

Salottolo K, Cole B, Bar-Or D. Intra-articular injection of the anti-inflammatory compound LMWF-5A in adults with severe osteoarthritis: a double-blind prospective randomized controlled multi-center safety and efficacy trial. Patient Saf Surg. 2018 Jun 18 — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of Participants Classified as Responders	Using the Outcome Measures in Rheumatology Clinical Trials and Osteoarthritis Research Society International (OMERACT-OARSI) criteria of WOMAC A Pain subscore, WOMAC C Function subscore, and PGA as composite endpoints. A patient in this study will be considered a responder for the purpose of efficacy analysis if the following criteria are met: (1) demonstration of = 50% improvement AND a 1.0-unit change in pain OR 1.0-unit change in function OR; If the patient does not meet this criterion, then the patient must demonstrate at least 2 of the following: Improvement in pain (WOMAC A) =20% and a 0.5 point absolute change in pain from Baseline on the 5-point Likert scale; Improvement in function (WOMAC C) =20% and a 0.5 point absolute change in function from Baseline on the 5-point Likert scale; Improvement in patient global assessment (PGA) =20% and a 0.5 point absolute change in function from Baseline on the 5-point Likert scale	Determined from Baseline to 12 Weeks