MAC Clinical Research
Manchester, United Kingdom
NCT Number: NCT04670289
This study is testing a drug called TenoMiR that is being developed for the treatment of tennis elbow (lateral epicondylitis). The study drug is a new compound that works by improving the quality of the collagen which helps repair damage to the elbow. The study drug is being developed in the hope of providing a more reliable treatment than those currently available and can be given at the time of first diagnosis, so that recovery can begin as soon as possible.
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Notify Me18 year–70 year
All sexes
Interventional
Phase 1
Manchester, United Kingdom
TenoMiR a chemically synthesised mimic of microRNA-29a (miR29a) which has improved stability, activity and cellular uptake while being non-immunogenic, has been created to restore miR29a levels back to pre-injury levels.
TenoMiR is unique in directly targeting the key changes in collagen production associated with tendinopathy. Unlike other therapies, TenoMiR has a well-defined mode-of-action that is supported by a wealth of scientific data. Moreover, treatment with TenoMiR does not require invasive biopsies and can be delivered at the point of initial diagnosis initiating recovery at the very earliest time.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Subjects with any of the following will be excluded from study participation:
Mimic of miR29a
Other names: CWT-001
Mimic of miR29a
Other names: CWT-001
Mimic of miR29a
Other names: CWT-001
0.9% saline
Time frame: 14 days
Comparison of clinical laboratory abnormalities between TenoMiR versus placebo as measured by blood chemistry, haematology, coagulation, serology and urinalysis.
Time frame: 14 days
Comparison of changes in vital signs between TenoMiR versus placebo as measured by supine vital signs including pulse rate, blood pressure, respiration rate and oral temperature.
Time frame: 14 days
Comparison of changes in 12 lead ECG parameters as measured by Heart Rate and PR, RR, QRS, QT and QT intervals.
Time frame: 14 days
Comparison of changes in physical examination between TenoMiR versus placebo as measured by height, BMI, and body weight, and assessments of the head, eyes, ears, nose, throat, skin, thyroid, neurological, lungs, cardiovascular system, abdomen (liver and spleen), lymph nodes and extremities.
Time frame: 14 days
Comparison of changes in skin score assessment of injection site between TenoMiR versus placebo as measured by for erythema, pain, tenderness and swelling.
Time frame: 90 days
Plasma PK by maximum drug plasma concentration (Cmax).
Time frame: 90 days
Plasma PK by time to reach Cmax (tmax).
Time frame: 90 days
Plasma PK by area under the plasma vs. concentration time curve (AUC).
Time frame: 90 days
Changes in pain score per group
Time frame: 90 days
Changes in Quick DASH per group
Time frame: 90 days
Changes in ASES-E per group
Time frame: 90 days
Changes in PRTEE per group
Time frame: 90 days
Change in analysis of focal hypoechoic areas within the tendon per group
Causeway Therapeutics
Industry
A Phase 1, Single-Centre, Randomised, Double-Blind, Placebo-Controlled Study Evaluating the Safety, Tolerability and Pharmacokinetics of Single Ascending Doses of TenoMiR Injections in Subjects With Lateral Epicondylitis
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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