Search clinical trials for: Juvista+%28avotermin%29

Total 146 results

Renovo

Completed

A Trial to Compare the Efficacy of Two Formulations of Avotermin Against Placebo (RN1006)

Scar Improvement

United Kingdom
Renovo

Completed

Anti-Scarring Efficacy and Safety of Intradermal Juvista (Avotermin) in Healthy Males

Cicatrix

United Kingdom
Renovo

Completed

Efficacy and Safety of Intradermal RN1001 (Avotermin) in Elderly Subjects.

Cicatrix

United Kingdom
Renovo

Completed

Exploratory Study of the Efficacy and Safety of Juvista 250ng When Administered Following Excision of Ear Lobe Keloids

Keloid

United States
Renovo

Completed

Juvista in Scar Revision Surgery of Disfiguring Scars (Revise)

Cicatrix

Spain, France, Hungary, Italy, United Kingdom, United States, Denmark, Germany, Latvia, Poland
Renovo

Completed

Safety and Efficacy Study of Avotermin (Juvista) in Female Subjects

Cicatrix | Wound Healing

United Kingdom
Renovo

Completed

Investigation of the Accelerated Healing and Anti-scarring Potential of Avotermin (Juvista) in Split Skin Graft Donor Sites

Cicatrix | Wound Healing

United Kingdom
Renovo

Completed

Safety Study of Repeated, Escalating Doses of Intradermal Avotermin (Juvista)

Cicatrix | Wound Healing

United Kingdom
Renovo

Completed

Investigation of the Safety, Dosing Frequency and Anti-Scarring Potential of Two Concentrations of Intradermal Avotermin (Juvista)

Cicatrix | Wound Healing | Re-epithelialization

United Kingdom
Renovo

Completed

Genomic Changes Associated With the Use of Intradermal Avotermin (Juvista) in Small Wounds in Healthy Male Subjects

Cicatrix | Wound Healing

United Kingdom
Renovo

Completed

Improvement in Scar Appearance Following Injection of Avotermin (Juvista) Into Skin Incisions Made in Healthy Men and Women

Cicatrix

United Kingdom
Renovo

Withdrawn

Juvista in the Non-surgical Improvement of Existing Scars

Scars

United Kingdom
Renovo

Completed

Scar-Improvement Efficacy and Safety of a Single Intradermal Injection of Avotermin (Juvista) Administered Following Full-Thickness Skin Incisions

Cicatrix

United Kingdom
Istanbul Medeniyet University

Completed

Turkish Validation and Reliability of LURN SI-29 Questionnaire in Patients With Lower Urinary Tract Symptoms

Lower Urinary Tract Symptoms | Urinary Incontinence

Turkey
Renovo

Unknown

Juvista (Avotermin) in the Prevention or Improvement of Scar Appearance Following Scar Revision Surgery.

Cicatrix

United Kingdom
Boston Scientific Corporation

Withdrawn

REPRISE EDGE 29 mm EU Study

Aortic Valve Stenosis
Renovo
ICON Clinical Research

Completed

Juvista (Avotermin) in Scars Following Varicose Vein Removal

Cicatrix | Varicose Veins

Belgium, United Kingdom, Latvia, Lithuania
Renovo

Completed

Trial of Juvista (Avotermin) Following Removal of Ear Lobe Keloid Scars

Keloid

United States
Renovo

Completed

RN1001(Avotermin) in Scar Improvement Following Breast Augmentation

Cicatrix | Mammaplasty

United Kingdom
Renovo

Terminated

Juvista (Avotermin) in Breast Reduction Surgery Scars

Cicatrix | Mammaplasty

United Kingdom
Renovo

Unknown

A Trial to Investigate Scar Improvement Efficacy of RN1001 (Avotermin) After Head and Neck Naevi Excision

Cicatrix | Nevus

United Kingdom
Legend Labz, Inc.

Recruiting

Effect of Different Ingestion Doses of Celastrol on Human Sperm Motility

Safety Issues

United States
ZymoGenetics

Completed

Study of PEG-rIL-29 (or PEG-IFN Lambda) in Subjects With Chronic Hepatitis C Virus Infection

Hepatitis C, Chronic

United States, Canada
Renovo

Completed

Safety of Juvista When Administered Following Excision of Ear Lobe Keloids (RN1001-0093)

Keloid

United States
Renovo

Completed

Safety and Efficacy of RN1001(Avotermin) in Healthy Male Subjects

Cicatrix

United Kingdom
Bausch & Lomb Incorporated

Completed

Evaluate the Safety and Effectiveness of the enVista® One-Piece Hydrophobic Acrylic Trifocal Intraocular Lens

Cataract

United States
M.D. Anderson Cancer Center

Recruiting

Hyperpolarized 129-Xenon Imaging in Adult Hematopoietic Cell Transplant Recipients With Pulmonary Impairment

Pneumonia | Hematopoietic System--Cancer | Pulmonary

United States
Vanderbilt-Ingram Cancer Center
National Cancer Institute (NCI)

Recruiting

Low-Dose Total Skin Electron Therapy in Treating Patients With Refractory or Relapsed Stage IB-IIIA Mycosis Fungoides

Recurrent Mycosis Fungoides | Refractory Mycosis Fungoides | Stage I Mycosis Fungoides | Stage II Mycosis Fungoides | Stage III Mycosis Fungoides

United States
Bausch & Lomb Incorporated

Completed

Retrospective Chart Review of enVista Toric 0.9D Intraocular Lenses

Corneal Astigmatism

Canada
Journey Medical Corporation
Dr. Reddy's Laboratories Limited

Completed

A Comparative Bioavailability Study of DFD-29 Capsules 40 mg Versus SOLODYN® Tablets 105 mg, Under Fasting & Fed Conditions in Healthy Adult Human Subjects

Pharmacokinetics

Canada
Merck Sharp & Dohme LLC

Completed

Safety, Pharmacokinetics, and Pharmacodynamics of Ruzasvir (MK-8408) in Participants With Hepatitis C Infection (MK-8408-003)

Hepatitis C Infection
Bausch & Lomb Incorporated

Completed

Hydrophobic Acrylic Toric IOL Designed to Reduce the Effects of Preoperative Corneal Astigmatism

Astigmatism

United States
Bausch & Lomb Incorporated

Completed

One-Piece Hydrophobic Acrylic Intraocular Lens in Subjects Undergoing Cataract Extraction

Cataract | Aphakia

United States
Bausch & Lomb Incorporated

Completed

Clinical Study to Evaluate the Safety and Performance of the enVista® One-Piece Hydrophobic Acrylic Trifocal Intraocular Lens in Subjects Undergoing Cataract Extraction

Cataract

Canada
Chongqing Precision Biotech Co., Ltd

Enrolling by invitation

Dual-target CAR-T Cells (C-4-29) in the Treatment of Relapsed/Refractory Multiple Myeloma

Multiple Myeloma in Relapse | Multiple Myeloma, Refractory

China
Legend Labz, Inc.

Recruiting

A Sub-Chronic Evaluation of the Safety of Celastrol in Human Subjects

Safety

United States
Bausch & Lomb Incorporated

Not yet recruiting

A Study to Evaluate the enVista® Aspire (EA) Intraocular Lens in Subjects Undergoing Cataract Extraction

Cataract
National Cancer Institute, Naples

Not yet recruiting

PRO for Fighting FT in Ovarian Cancer (MITO45-ProFFiT)

Ovarian Cancer

Italy
Hacettepe University

Completed

Serum Fibroblast Growth Factor-21 Levels During Prolonged Fasting

Fasting | Fibroblast Growth Factor-21

Turkey
Journey Medical Corporation
Dr. Reddy's Laboratories Limited

Completed

A Randomized, Double-Blind Study to Assess the Safety, Efficacy and Tolerability of Oral DFD-29 Capsules for the Treatment of Rosacea. (MVOR-1)

Papulopustular Rosacea

United States
University of South Carolina
Susan G. Komen Breast Cancer Foundation

Completed

Brown Seaweed as a Breast Cancer Preventive

Breast Cancer

United States
Dr. Reddy's Laboratories Limited

Completed

A Controlled Study to Assess the Efficacy, Safety and Tolerability of Oral DFD-29 Extended Release Capsules

Rosacea

Germany
Providence Health & Services

Completed

Phase 1 Study of Anti-OX40 in Patients With Advanced Cancer

Advanced Cancer

United States
Balt Extrusion

Active, not recruiting

Safety and Efficacy of Silk Vista and Silk Vista Baby Flow Diverter for Intracranial Aneurysm Treatment (FIRST)

Intracranial Aneurysm

Spain, Israel, Croatia, France, Italy, Austria, Belgium, Germany, Netherlands
Journey Medical Corporation
Dr. Reddy's Laboratories Limited

Completed

Impact of DFD-29 on Microbial Flora of Healthy, Adult Human Subjects When Administered Over 16 Weeks

Rosacea

United States
University Hospital, Grenoble

Recruiting

Study Evaluating the Effectiveness of Treatment With Vista Care®, in Arterial Ulcers of the Lower Extremities (VISTA CARE)

Wound Heal

France
Journey Medical Corporation
Dr. Reddy's Laboratories Limited

Completed

A Study to Assess the Safety, Efficacy and Tolerability of Oral DFD-29 Capsules for the Treatment of Rosacea (MVOR-2) (MVOR-2)

Papulopustular Rosacea

United States, Germany
Bausch & Lomb Incorporated

Not yet recruiting

Study to Evaluate the Safety and Effectiveness of the enVista® Beyond (EY) EDF Intraocular Lens in Subjects Undergoing Cataract Extraction

Cataract

United States, Canada
VISTA Ophthalmics
CBCC Global Research

Active, not recruiting

A Study to Evaluate the Safety and Performance of the Vista Probe for Vitrectomy Surgery

Vitrectomy

United States
NYU Langone Health

Withdrawn

Gut Microbiome Modulation to Enable Efficacy of Checkpoint-based Immunotherapy in Pancreatic Adenocarcinoma

Pancreatic Cancer

United States

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