Clinical Trial Finder

Inclusion Criteria:

1. Age eligible for study: 21 to 75 years. 2. Gender eligible for study: All. 3. Study subjects must be willing to give written informed consent to participate in the study and sign the Health Insurance Portability and Accountability Act (HIPAA) authorization before any study procedures are performed. 4. Subjects have a diagnosis of OA in at least one knee defined as Grade II or III on Kellgren-Lawrence (K-L) grading scale which is confirmed by posterior-anterior, weight-bearing, fixed flexion radiography with 10o caudal beam angulation. 5. Subjects with VAS pain score ≥40 mm on screening day will be included. 6. Subjects had one or more of the following SOC treatments within the previous 12 months will be included: 1. weight loss. 2. physical therapy. 3. anti-inflammatory medications

• - oral, injections and topical.

7. Body mass index (BMI) < 45kg/m2. 8. Subjects must be available for all specified assessments at the study site through the completion of the study. 9. For Women of Child-Bearing Potential (WOCBP) only, willingness to use FDA-recommended birth control until 6 months post treatment. The FDA-approved and cleared methods for birth control are listed below: 1. Permanent Sterilization. 2. Long-Acting Reversible Contraceptives (LARC) 3. Contraceptive Injection. 4. Short-Acting Hormonal Methods. 5. Barrier Methods. 6. Emergency Contraception https://www.fda.gov/consumers/free-publications-women/birth-control. 10. Any male subject must agree to use contraceptives and not donate sperm during the study. 11. Patient may be eligible for treatment of both knees if criteria is met for both.

Exclusion Criteria:

1. Subjects have evidence of significant and unstable cardiac dysfunction, e.g. acute myocardial infarction and hypertension with uncontrolled blood pressure over 140/90 will be excluded. 2. Subjects at screening with white blood cell count < 4 x 109 cells/L, hematocrit <30%, and platelets <150 x 109 /L will be excluded. 3. Subjects with poorly controlled diabetes (hemoglobin A1C > 7.5 or fasting blood glucose of >200) in last 6 months will be excluded. 4. Individuals on dialysis or uncontrolled renal disease will be excluded. 5. Subjects with abnormal hematology, serum chemistry, or urinalysis screening laboratory results will be excluded. 6. Subjects with history of, or ongoing, autoimmune disorder that requires treatment with an immunosuppressive medication will be excluded. 7. Subjects had knee surgery on the targeted knee within 12 months prior to screening and /or planned knee surgery during the study will be excluded. 8. Subjects have a body mass index greater than 45 kg/m2 will be excluded. 9. Subjects whose knee pain is caused by, (i) diffuse edema, extra articular causation (ii) displaced meniscus tear, (iii) full thickness articular cartilage lesion greater than 1 cm in any direction, or (iv) osteochondritis dissecans will be excluded. 10. Subjects have rheumatoid arthritis, psoriatic arthritis, or have been diagnosed with any other auto-immune disorders that could be the cause of their knee pain will be excluded. 11. Subjects which have evidence or history of malignancy except those who are successfully treated in situ or basal cell skin cancers will not be excluded. 12. Subjects with a history of clotting disorder, anticoagulation therapy that cannot be stopped as prior to infusion will be excluded. 13. Subjects have evidence of liver dysfunction manifested as alkaline phosphatase greater than 345 u/L, total bilirubin greater than 1.65 mg/dL, ALT greater than 275 units/L and/or AST great than 240 units/L will be excluded. 14. Subjects have or had an active infection requiring systemic antibiotics within 2 weeks on enrollment in the study will be excluded. 15. Subjects currently taking anticoagulant therapy (excluding Plavix or Aspirin) will be excluded. 16. Subjects have received an intra-articular hyaluronic acid (HA) or platelet rich plasma (PRP) for the treatment of OA of the target knee within 12 weeks prior to screening will be excluded. 17. Subjects have used an investigational drug or had surgical intervention within 12 weeks of the study enrollment will be excluded. 18. Subjects that are unwilling to stop taking prescription or over the counter pain medication for Osteoarthritis for 7 days prior to any visit will be excluded. Subjects will be permitted to take medications for non-osteoarthritis condition (excluding the one's listed under "Concomitant Medication"). 19. Subjects needing or at high risk of requiring systemic steroids during the course of study will be excluded except systemic use of corticosteroid administration for COVID-19 or flare up of non-arthritic condition. Complete information of dose and timeframe of the medication use will be documented in case report forms (CRF). 20. Be a female who is pregnant, nursing, or of childbearing potential while not practicing effective contraceptive methods. 21. Subjects who are unable to complete all the testing required for the study will be excluded. 22. Subjects on active listing (or expected future listing) for transplant of any organ will be excluded. 23. Be a solid organ transplant recipient. This does not include prior cell-based therapy (>12 months prior to enrollment), bone, skin, ligament, tendon or corneal grafting. Have a history of organ or cell transplant rejection. 24. Subjects with history of drug abuse (illegal "street" drugs except marijuana (If it is legal use in states where patient resides), or prescription medications not being used appropriately for a pre-existing medical condition or alcohol abuse (≥ 5 drinks/day for ˃ 3 months). 25. Subjects with untreated HIV infection will be excluded. However, patients can be enrolled if have been treated for HIV and the test negative for HIV viral load but still test positive for antibodies. 26. Subjects with neural or vascular claudication or neurologic disorder including, but not limited to epilepsy, Parkinson's disease, dementia, cerebrovascular disease, tumor of the nervous system, and amyotrophic lateral sclerosis will be excluded. 27. Subjects cannot have had a hyaluronic acid injection within 6 months prior to NANOVAE injection. 28. Subjects cannot have had a cortisone injection within 3 months prior to NANOVAE Injection

The investigational product being assessed in this trial is called NANOVAE, which is a biologic derived from human amniotic fluid (HAF) that is allogenic and acellular. HAF contains a wide range of growth factors, cytokines, chemokines, and extracellular vesicles/nanoparticles obtained from perinatal tissue. These components contribute to the regenerative potential of HAF and make it a promising option for regenerative medicine applications, particularly in knee osteoarthritis (KOA). Studies have demonstrated that the extracellular vesicles found in HAF, including exosomes, have the ability to promote chondrogenesis and reduce inflammation, which are crucial processes in reversing the progression of KOA. Additionally, these vesicles have shown to stimulate cartilage regeneration, addressing the impaired cartilage repair typically observed in OA. Therefore, the administration of HAF-derived products has the potential to slow down the degenerative process and promote cartilage repair in patients with KOA. The growth factors and cytokines present in HAF may also help alleviate the inflammatory response observed in the knee joint, a characteristic feature of KOA. These anti-inflammatory properties, combined with the regenerative capabilities of the extracellular vesicles, make HAF an appealing candidate for the treatment of KOA. Numerous clinical studies registered under ClinicalTrials.gov have provided evidence of the safety and effectiveness of HAF products in joint therapies. The use of HAF for treating OA holds immense potential due to its array of growth factors, anti-inflammatory mediators, and medicinal signaling cells, which continue to undergo rapid advancements. In a non-FDA review study, a double-blinded controlled trial was conducted comparing the treatment of OA with freshly collected amniotic fluid and steroids. The results revealed a significant improvement in the Visual Analog Scale (VAS) after three months of treatment, with continuous improvement in VAS after six months in both groups. However, the group receiving freshly collected amniotic fluid exhibited greater improvement. These findings strongly support the potential of this novel HAF therapy for advanced OA, as it proved to be superior and longer lasting compared to conventional therapies commonly practiced. Further research, both in terms of basic science and clinical investigations, is warranted to gain a better understanding of the anti-inflammatory properties of amniotic fluid and determine the most efficacious amniotic fluid product for symptomatic OA. NANOVAE is a filtered form of HAF (human amniotic fluid) that utilizes the wide range of nanoparticles, cytokines, and growth factors present in the fluid, which play vital roles in fetal development and maturation. HAF is a rich source of collagen substrates, growth factors, amino acids, polyamines, lipids, carbohydrates, cytokines, and extracellular matrix molecules like hyaluronic acid and fibronectin, as well as cells. These components greatly contribute to tissue protection and repair. Extensive research has demonstrated the antimicrobial, immunomodulatory, and growth-promoting properties of HAF. The antimicrobial, antiviral, and antifungal effects of HAF have been established through the identification of various components such as lysozyme, peroxidase, transferrin, β-lysin, immunoglobulins, and zinc-peptide complexes within the fluid. The immunomodulatory functions of HAF have been observed in its ability to suppress alloreactive responses and downregulate Th1 and Th2 cytokines. NANOVAE's extracellular vesicle (EV) fraction consists of several cytokines, chemokines, and growth factors that are associated with functions such as host defense, anti-inflammatory response, angiogenesis, and cartilage repair. The concentration of nanoparticles in the final product has been consistently demonstrated through nanoparticle analysis using the ZetaView Quatt nanoparticle analyzer. This analysis reveals a range of particles, with an average mode particle size of 96.4 nM, which aligns with the expected size of exosomes ranging between 50-200 nm in diameter. Objectives: Primary Objective: To demonstrate the safety of NANOVAE administered intraarticular in subjects with KOA by measuring the incidence of any of the following treatment-emergent adverse events (TE-AEs) and treatment-emergent serious adverse events (TE-SAEs) within the first 30 days of injection: Occurrence of adverse events related to the therapy within 30 days of NANOVAE treatment. Life-threatening event (e.g., stroke or non-fatal pulmonary embolism). Event resulting in persistent or significant disability/incapacity. Event resulting in death. Secondary Objective: To demonstrate the potential efficacy of NANOVAE by measuring the following clinical response changes from baseline to 12 months after injection. Time Frame: Month 1, 3, 6, and 12 after infusions: Change in single leg stance test. Change in "Timed Up and Go" test to assess fall risk. Change in Western Ontario and McMaster Universities Osteoarthritis (WOMAC) Index (five items for pain, two for stiffness, and seventeen for function). Change in range of motion, assessed by goniometer measurements. Change in serum and/or synovial biomarkers between the timepoints of Day 0 and the 3-month visit. Design and Investigational Plan: A total of 24 subjects meeting all inclusion/exclusion criteria will be divided into two groups. Group 1 will be an open-label lead-in phase. Group 2 will be a randomized, double-blinded, placebo-controlled cohort. Group 1 will receive one dose of 2ml of NANOVAE, and Group 2, in a randomized and double-blinded fashion, will receive two doses of 2ml NANOVAE. Neither the patients nor the researchers will know who is getting the placebo and who is getting the NANOVAE; only the product manufacturing staff will be unblinded. The ratio of placebo to NANOVAE is 1:1 for a total of 16 subjects in Group 2. Only the knee with the more severe symptoms of OA will be treated. The allogenic-HAF will be obtained from healthy donors and manufactured by the Nova Vita Laboratories processing lab. Group 1 (Open Label): A total of eight subjects will be treated to assess safety prior to enrolling Group 2. Safety will be assessed at seven-day intervals for the 8 subjects in Group 1, staggered by 5 days after receiving the dose of NANOVAE. Dose: 2 mL of NANOVAE on Day 0 containing 1.0 x 10¹¹ to 9.0 x 10¹¹ particles/ml. Product will be administered directly without any dilution. After these 8 subjects complete the 5-day safety assessment, the safety report will be presented to the DSMB with representative data to determine the safety status of receiving one dose of NANOVAE. Once the treatment of Group 1 has been determined to be safe, the enrollment of Group 2 will begin. Group 2 (Randomized, double-blinded placebo control): A total of sixteen subjects will be randomized to either receive two doses of NANOVAE via intraarticular injections or receive two doses of a placebo. Dose: 2 mL of NANOVAE or placebo on Day 0 and Day 15, containing 1 x 10¹¹ particles/ml. The ratio is 1:1 for a total of 16 subjects in Group 2. Product will be administered directly without any dilution. Sample Size & Study Population: A total of 24 adult patients will be chosen from the population of adults between the ages of 21 to 75 diagnosed with KOA who meet inclusion criteria. Route of Administration: Intra-articular Injections. Study Duration and Study Follow-Up: 12 months total duration: Day 0 and 15

• - Intraarticular Injection and observational follow-up.

Days 1 and 7 (after dose of NANOVAE or placebo)

• - Observational follow-up via phone call, telehealth, or in-person visit.

Months 1, 3, 6, and 12

• - Observational follow-up visits per protocol design.

Arms

Experimental: Group 1 (Open Label)

A total of eight subjects will be treated to assess safety prior to enrolling Group 2. We propose to assess the safety of 8 subjects in Group 1 at seven-day intervals. Each subject in Group 1 will be staggered by 5 days after receiving the dose of NANOVAE. Dose - 2 mL of NANOVAE on day 0 containing 1.0 x 1011 to 9.0 x 1011 particles/ml. Product will be administered directly without any dilution.

Experimental: Group 2 (Randomized, double blinded placebo control)

Total of sixteen subjects will be randomized to either receive two doses of NANOVAE via intraarticular injections or receive two doses of a placebo. Dose - 2 mL of NANOVAE or placebo on day 0 and day 15, containing 1 x 1011 particles/ml. The ratio is 1:1 for a total of 16 subjects in the Group 2. Product will be administered directly without any dilution.

Interventions

Drug: - NANOVAE - Acellular Allogenic Human Amniotic Fluid (hAF)

A total of 24 subjects meeting all inclusion/exclusion criteria will be divided into two groups. Group 1 will be an open-label lead-in phase. Group 2 will be a randomized, double-blinded, placebo-controlled cohort. Group 1 will receive one dose of 2ml of NANOVAE, and Group 2, in a randomized and double-blinded fashion, will receive two doses of 2ml NANOVAE. Neither the patients nor the researchers will know who is getting the placebo and who is getting the NANOVAE; only the product manufacturing staff will be unblinded. The ratio of placebo to NANOVAE is 1:1 for a total of 16 subjects in Group 2. Only the knee with the more severe symptoms of OA will be treated. The allogenic-HAF

Drug: - 0.9% Sodium Chloride Injection, USP

In lieu of AF, the saline for injection will be used as a placebo. Vials acquired from the manufacturer is pipetted into glass vials, stoppered, capped, placed in labeled header foil pouches, and sealed. These are transferred to a quarantine freezer to await post-production testing.