Safety Study of PTP-001 for Treating Knee Osteoarthritis

Knee Osteoarthritis Clinical Trial

Official title:

A Prospective, Open-Label, Dose-Escalation Phase 1 Study of Intra-Articular Administration of an Allogeneic Human Placental Tissue Particulate (PTP-001) for the Treatment of Knee Osteoarthritis

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT04632966
• Other study ID #: KOA-20-01
• Status: Active, not recruiting
• Phase: Phase 1
• Start date: February 26, 2021
• Est. completion date: December 2022

Study information

• Verified date: December 2021
• Source: Bioventus LLC
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Evaluation of safety, tolerability, and efficacy of a single intra-articular (IA) injection of PTP-001, an allogeneic placental tissue particulate, in individuals with knee osteoarthritis (OA).

Description:

This open-label, dose-escalation study is expected to enroll 20 participants, 40-80 years of age and test two doses (low and high dose) of PTP-001, an allogeneic placental tissue particulate, in two unique cohorts of 10 participants each. Each participant will receive a single intra-articular (IA) injection of PTP-001. Following the completion of the first cohort in which 10 participants (Kellgren-Lawrence Grade 2 or 3 knee OA) will be treated with the low dose of PTP-001, safety data will be reviewed by an independent Data and Safety Monitoring Board (DSMB).

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 20
• Est. completion date: December 2022
• Est. primary completion date: September 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 40 Years to 80 Years

Eligibility

Inclusion Criteria:

• Written consent to participate in the study

• Male or female, aged 40 to 80 years

• Symptomatic knee OA with Kellgren-Lawrence radiographic classification of 2 or 3

• Non-responsive after at least 3 months of conservative therapy for knee OA

• Females of childbearing potential must have negative pregnancy test result prior to treatment and must commit to highly effective methods of contraception for at least 6 months after treatment

• Willingness to report oral analgesic treatment used for knee pain and to discontinue analgesic treatment for knee pain in 24 hours prior to each study visit

• Willingness to limit use of pain rescue medication to oral acetaminophen for management of painful knee OA flare

Exclusion Criteria:

• Body mass index (BMI) = 40 kg/m2 or BMI = 35 kg/m2 with condition that warrants weight loss surgery

• Presence of active infection of index knee or systemic infection requiring treatment within 3 months of Screening

• Administration of IA injection within 3 months of Screening

• Significant acute injury to index knee within 3 months of Screening

• Surgery to index knee within 6 months of Screening or planned surgery to index knee within 6 months after Screening

• Unstable index knee joint

• History of radiation therapy of index knee

• Known vascular or neurological disorder affecting the index knee

• Osteonecrosis of either knee

• Clinical diagnosis of inflammatory arthritis

• Clinical diagnosis of autoimmune disease affecting the musculoskeletal system

• Use of any other investigational therapy within 3 months of Screening or planned for the duration of the study

• Current anti-coagulant use

• History of receiving a solid organ or hematologic transplant

• History of malignancy or radiotherapy within 5 years of Screening, except for basal or squamous cell carcinoma of the skin

• Use of immunosuppressive or chemotherapeutic agents within 5 years of Screening

• Known allergy to local anesthetics or allograft tissues

• Known history of hepatitis

• Known history of thrombotic or thromboembolic phenomena.

• Known history of primary or secondary immunodeficiency disorders

• Presence of concurrent medical condition that, in the investigator's judgement, could compromise participant safety or interfere with the required study assessments and study participation.

Note: Other protocol defined inclusion/exclusion criteria apply.

Related Conditions & MeSH terms

• Knee Osteoarthritis
• Osteoarthritis
• Osteoarthritis, Knee

Intervention

Biological:
• Biological: PTP-001
allogeneic placental tissue particulate

Locations

Country	Name	City	State
United States	James R. Urbaniak, MD, Duke Sports Science Institute	Durham	North Carolina
United States	Coastal Carolina Research Center	North Charleston	South Carolina

Sponsors (1)

Lead Sponsor	Collaborator
Bioventus LLC

Country where clinical trial is conducted

United States, 

References & Publications (2)

Flannery CR, Seaman SA, Buddin KE, et al. Characterization and preclinical efficacy of PTP-001, a novel human tissue biologic in development for the treatment of OA. Osteoarthritis Cartilage. 2020 Apr;28(Supplement 1):S487-S489. doi: 10.1016/j.joca.2020.02.763

Flannery CR, Seaman SA, Buddin KE, Nasert MA, Semler EJ, Kelley KL, Long M, Favret J, Pavesio A, Loeser RF. A novel placental tissue biologic, PTP-001, inhibits inflammatory and catabolic responses in vitro and prevents pain and cartilage degeneration in a rat model of osteoarthritis. Osteoarthritis Cartilage. 2021 Aug;29(8):1203-1212. doi: 10.1016/j.joca.2021.03.022. Epub 2021 May 20. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Change from baseline in biochemical markers (CTX-II & PRO-C2)	Urinary CTX-II samples; Serum PRO-C2 samples	Baseline to Week 52
Other	Change from baseline in joint space width of the index knee, assessed radiographically (OARSI radiographic scoring)		Baseline to Week 52
Primary	Incidence of local and systemic treatment emergent adverse events (AEs) and incidence of abnormal laboratory and immunogenicity panels	Incidence of local and systemic treatment emergent adverse events (AEs), including clinical laboratory and immunogenicity panels, after a single intra-articular injection of PTP-001.	Baseline to Week 52
Secondary	Western Ontario and McMaster University (WOMAC) Pain Responder Rate		Week 26 and Week 52
Secondary	WOMAC Physical Function Responder Rate		Week 26 and Week 52
Secondary	Change from baseline in pain of the index knee, by evaluating the WOMAC Pain subscale score (the possible total score ranging from 0-50 for pain)	WOMAC Numerical Rating Scale (NRS) 3.1 questionnaire is a health status measure questionnaire of 24 questions comprising 3 subscales (pain, stiffness and physical function). WOMAC A (measure of pain) is measured on 11-point NRS ranging from 0 (none) to 10 (extreme), where higher score represents higher pain.	Baseline to Week 52
Secondary	Change from baseline in physical function of the index knee, by evaluating the WOMAC Physical Function subscale score (the possible total score ranging from 0-170 for Physical Function)	WOMAC Numerical Rating Scale (NRS) 3.1 questionnaire is a health status measure questionnaire of 24 questions comprising 3 subscales (pain, stiffness and physical function). WOMAC C (measure of physical function) is measured on 11-point NRS ranging from 0 (none) to 10 (extreme), where higher score represents higher pain.	Baseline to Week 52
Secondary	Change from baseline in patient global assessment of OA, by assessing the participants assessment of how they are doing considering arthritis in index knee (the possible answers include "Very Good", "Good", "Acceptable", "Poor", "Very Poor"		Baseline to Week 52
Secondary	Change from baseline in health-related quality of life, by assessing the items from the Short Form 36 (SF-36) survey	The SF-36 measures 8 domains: physical functioning, role physical, bodily pain, general health, vitality, social functioning, role emotional, and mental health (the possible total normalized score ranges from 0-100). Higher scores on the SF-36 indicate better health status.	Baseline to Week 52