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NGI226 for Achilles Tendinopathy
Phase 2
Recruiting
Research Sponsored by Novartis Pharmaceuticals
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to day 169 (end of study)
Summary
This trial is testing an injection called NGI226 MP for people with a specific type of Achilles tendon injury. The goal is to see if this injection can make the injured tendon stronger and more flexible. Researchers will compare the results to ensure safety and effectiveness.
Who is the study for?
This trial is for individuals with mid-portion Achilles tendinopathy lasting over 8 weeks but less than a year, who haven't improved after at least 6 weeks of standard treatments like physiotherapy or NSAIDs. It's not suitable for those with conditions affecting injection safety, history of blood clots or frequent infections, past ankle surgeries or significant heart disease.
What is being tested?
The study is testing the safety and effectiveness of NGI226 Microparticles given as a single peritendon injection to improve Achilles tendon mechanical properties compared to a placebo in patients with Achilles tendinopathy.
What are the potential side effects?
While specific side effects are not listed, potential risks may include local reactions at the injection site such as pain, swelling, and irritation. Systemic side effects could occur but would depend on individual patient responses.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to day 169 (end of study)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to day 169 (end of study)
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Number of participants with AEs and SAEs
Secondary study objectives
Changes in tendon stiffness from baseline at week 12 assessed by ultrasound (US)-based shear wave elastography (SWE)
Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: NGI226Experimental Treatment1 Intervention
single peritendon injection
Group II: PlaceboPlacebo Group1 Intervention
single peritendon injection
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for Achilles Tendinopathy, such as peritendon injections, aim to improve tendon mechanical properties and reduce pain. These injections often contain substances like corticosteroids, platelet-rich plasma (PRP), or investigational agents like NGI226 MP.
The primary mechanism involves reducing inflammation, promoting tissue repair, and enhancing the structural integrity of the tendon. For Achilles Tendinopathy patients, this matters because improving tendon strength and flexibility can significantly reduce pain and improve function, facilitating a quicker return to daily activities and sports.
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Who is running the clinical trial?
Novartis PharmaceuticalsLead Sponsor
2,909 Previous Clinical Trials
4,210,023 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I don't have conditions that risk safety of tendon injections.I have Achilles tendinopathy diagnosed by a doctor and confirmed by ultrasound or MRI, with symptoms lasting more than 8 weeks but less than 12 months.I have had a severe Achilles tendon injury.I frequently get infections, including cold sores or genital herpes.I have a history of serious heart or blood vessel problems.My Achilles tendinopathy hasn't improved after 6 weeks of treatments like physiotherapy.I have had blood clots or conditions that increase my risk of clotting.I have had surgery for tendon issues or ankle problems.
Research Study Groups:
This trial has the following groups:- Group 1: NGI226
- Group 2: Placebo
Awards:
This trial has 0 awards, including:Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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