Clinical Trials Sponsored by Inge Tetens

Total 648 results

Inje University

Completed

Efficacy, Safety and Tolerability of Split-dose of PEG Compared With NaP Solution for Colonoscopy Preparation: A Randomized, Controlled Trial (SPEN)

Bowel Preparation, Efficacy, Tolerability, Safety

Korea, Republic of
Inje University

Completed

The Efficacy and Safety of Dexibuprofen Syrup

Fever | Respiratory Tract Infection

Korea, Republic of
Inje University

Completed

Bone Density in Patients With Schizophrenia

Schizophrenia | Alcohol Abuse

Korea, Republic of
Inge Marie Svane
Adaptimmune

Not yet recruiting

To Evaluate the Safety and Efficacy of ADP-TILIL7 in Patients With Locally Advanced or Metastatic Melanoma (ADP-TILIL7)

Melanoma | Melanoma Stage IV | Melanoma Stage III
Inge Holm
Herlev Hospital

Completed

The Effect of Endurance Training in Patients With Prostate Cancer

Prostate Cancer | Body Composition, Beneficial | Insulin Sensitivity

Denmark
Tethis S.p.A.

Recruiting

Evaluation of See.d as an Automated Blood Sample Preparator for Multiple Liquid Biopsy Applications

Breast Cancer | Healthy Participants

Italy
Tethis S.p.A.

Recruiting

Feasibility Study Aiming at Pre-Analytical Standardization of Whole Blood Processing for Liquid Biopsy Applications

Healthy Participants

Italy
Tethis S.p.A.

Recruiting

Identification of Breast Cancer Specific Markers in Patients Compared to Healthy Participants

Breast Neoplasms

Italy
Tethis S.p.A.

Recruiting

Identification of Prostate Cancer Specific Markers in Patients Compared to Healthy Participants

Prostatic Neoplasms

Italy
Tereos
BioFortis

Active, not recruiting

Study to Assess the Effects of Non Digestible Carbohydrates on Long-Term Glucose Homeostasis in Untreated Prediabetic Subjects (FOS_GLUCOSE)

PreDiabetes | Prediabetic State | Pre Diabetes | Dysglycemia

France
Dr. Inge Winter
Universität Münster

Recruiting

The Effect of a Six Week Intensified Pharmacological Treatment for Bipolar Depression Compared to Treatment as Usual in Subjects Who Had a First-time Treatment Failure on Their First-line Treatment. (INTENSIFY BD)

Bipolar Depression

Austria, Germany, Italy, Spain, United Kingdom
Dr. Inge Winter
Universität Münster

Recruiting

The Effect of a Six Week Intensified Pharmacological Treatment for Major Depressive Disorder Compared to Treatment as Usual in Subjects Who Had a First-time Treatment Failure on Their First-line Treatment. (INTENSIFY MDD)

Major Depressive Disorder | Treatment Resistant Depression

Austria, Germany, Italy, Spain, United Kingdom
Dr. Inge Winter
Universität Münster

Not yet recruiting

Intensified Pharmacological Treatment for Schizophrenia, Major Depressive Disorder and Bipolar Depression After a First-time Treatment Failure (INTENSIFY)

Bipolar Depression | Major Depressive Disorder | Schizophrenia and Related Disorders

Israel
Hinge Health, Inc

Active, not recruiting

HFIT Versus TENS Study for Chronic Low Back and Knee Pain

Chronic Pain | Knee Pain Chronic | Back Pain, Low

United States
Inje University
Allergan

Unknown

Effect of Dexamethasone Implant in Hard Exudate Complicated With Diabetic Macular Edema

Diabetes Mellitus | Macular Edema | Retinal Exudates and Deposits

Korea, Republic of
Inje University
GlaxoSmithKline

Unknown

Costs of Lost Productive Time Among Korean Workers With Panic Disorder and Effect of Treatment With Paroxetine Controlled Release

Panic Disorder

Korea, Republic of
Dr. Inge Winter
Universität Münster

Recruiting

The Effect of a Six Week Intensified Pharmacological Treatment for Schizophrenia Compared to Treatment as Usual in Subjects Who Had a First-time Treatment Failure on Their First-line Treatment. (INTENSIFY SZ)

Schizophrenia and Related Disorders | Early Treatment-Resistance

Austria, Germany, Italy, Spain, United Kingdom
Inje University
Sanofi

Completed

The Effects of Nateglinide and Acarbose on the Post-Prandial Glucose Control in Type 2 Diabetic Patients

Diabetes Mellitus | Type 2 Diabetes Mellitus

Korea, Republic of
Tereos
CEN Biotech

Completed

Evaluation of Gastrointestinal Comfort Following Regular Consumption of Short-chain Fructo-oligosaccharides (10-20 g Per Day) by Children Aged 6-12 Years (FOSTI)

Gastrointestinal Tract

France
Statens Serum Institut

Completed

A Trial in Subjects Suspected to Have Tuberculosis, Comparing the Diagnostic Performance of C-Tb to QuantiFERON®, in Combination With a Safety Assessment of C-Tb Versus Tuberculin PPD RT23 SSI

Tuberculosis

South Africa
Statens Serum Institut

Completed

Comparison of Diagnostic Performance of C-Tb to QuantiFERON®-TB, in Combination With a Safety Assessment of C-Tb vs Tuberculin PPD RT23 SSI

Tuberculosis

Spain
Statens Serum Institut

Completed

Safety and Risk of Sensitisation of the rdESAT-6 + rCFP-10 Skin Test Following Repeated Intradermal Administration

Tuberculosis

Denmark
Statens Serum Institut

Completed

A Safety and Immunogenicity Trial With an Adjuvanted Tuberculosis(TB) Subunit Vaccine (THYB-01)

Tuberculosis

Netherlands
Statens Serum Institut

Completed

A Trial of the C-Tb Skin Test, When Given Intradermally to Healthy Volunteers Previously Vaccinated With BCG (TESEC-03)

Tuberculosis

United Kingdom
Statens Serum Institut

Completed

A Safety and Immunogenicity Trial With an Adjuvanted TB Subunit Vaccine (Ag85B-ESAT-6 + IC31) (THYB-03)

Tuberculosis
Statens Serum Institut

Completed

Safety Study Investigating if Concomitant Injections of C-Tb and 2 T.U Tuberculin Affect Induration Responses (TESEC-07)

Tuberculosis

South Africa
Tethys Bioscience, Inc.

Unknown

Prospective Observational Study Assessing Treatment and Outcomes of Patients With Prediabetes

Prediabetes
Statens Serum Institut

Completed

Immunogenicity and Safety of Tetanus, Diphtheria and Mono Component Acellular Pertussis (TdaP) Vaccine in Comparison to Tetanus and Diphtheria (Td) Vaccine When Given as Booster Vaccinations to Adults

Healthy

Denmark
Terns, Inc.

Completed

AVIATION Study: A Safety, Pharmacokinetics, Pharmacodynamics and Preliminary Efficacy Study of TERN-201 in Patients With Non-Cirrhotic Non-Alcoholic Steatohepatitis

NASH - Nonalcoholic Steatohepatitis

United States
Tetec AG

Completed

Safety and Efficacy With NOVOCART® Disc Plus (ADCT) for the Treatment of Degenerative Disc Disease in Lumbar Spine (NDisc)

Intervertebral Disc Displacement | Intervertebral Disc Degeneration

Germany, Austria
Inge Nygaard Pedersen
Aalborg University

Unknown

Music Therapy Towards Schizophrenia, Negative Symptoms

Schizophrenia

Denmark
Inge Holm
The Augustinus Foundation, Denmark.

Unknown

Marathon Runners Compared to Sedentary Matched Control Subjects

Type 2 Diabetes

Denmark
Recens Medical, Inc.

Completed

Long Term Safety of Cooling Anesthesia for Intravitreal Injection (COOL-2)

Macular Degeneration | Diabetic Retinopathy | Diabetic Macular Edema | Macular Edema | Anesthesia, Local | Intravitreal Injection

United States
Recens Medical, Inc.

Completed

Cooling Anesthesia for Intravitreal Injection (COOL-1)

Macular Degeneration | Diabetic Macular Edema | Anesthesia, Local | Intravitreal Injection

United States
Statens Serum Institut

Completed

A Trial of the C-Tb Skin Test, When Given Intradermally to Adult Patients Recently Diagnosed With Active Tuberculosis (TB) (TESEC-04)

Tuberculosis

South Africa
Statens Serum Institut

Completed

Treatment Study of Metronidazole to Treat Dientamoebiasis in Children (DFPT)

Dientamoebiasis

Denmark
Statens Serum Institut

Completed

A Safety and Dose Finding Trial of C-Tb, When Given to Adult Patients Recently Diagnosed With Active Tuberculosis (TESEC-02)

Tuberculosis

United Kingdom
Statens Serum Institut

Completed

Trial on the Safety of a New Liposomal Adjuvant System, CAF01, When Given With the Tuberculosis Subunit Vaccine Ag85B-ESAT-6 as Two Injections With Two Months Interval to Healthy Adult Volunteers

Tuberculosis

Netherlands
Statens Serum Institut

Completed

Safety and Immunogenicity of a New Serum-free DTaP-IPVvero Combination Vaccine

Active Immunization

Poland
Statens Serum Institut

Completed

A Safety and Immunogenicity Trial With an Adjuvanted Tuberculosis (TB) Subunit Vaccine in Purified Protein Derivative (PPD) Positive Volunteers (THYB-02)

Tuberculosis

Netherlands
Tetec AG

Active, not recruiting

Phase III Study to Evaluate Safety and Effectiveness of NOVOCART 3D Plus vs. Microfracture in Knee Cartilage Defects (N3D)

Traumatic Articular Cartilage Defects in the Knee Joint

United Kingdom, Hungary, Czechia, Germany, Lithuania, Austria, France, Latvia, Poland, Switzerland
Tetec AG

Active, not recruiting

NOVOCART® Inject Plus for Cartilage Defects of the Knee

Cartilage Defects of the Knee

Lithuania, Hungary, Czechia, Germany, Switzerland
Sira Bang

Completed

Anticholinergic Premedication for Sedation With Dexmedetomidine During Spinal Anesthesia

Bradycardia

Korea, Republic of
Inje University
Bukwang Pharmaceutical

Terminated

Efficacy of Clevudine Plus Lamivudine for Lamivudine-resistant Chronic Hepatitis B Patients

Chronic Hepatitis B

Korea, Republic of
Yonsei University
Inje University

Completed

Study of Cytochrome P450 Polymorphisms (CYP2D6, CYP3A4/5 and CYP2C19) in Breast Cancer Patients

Breast Neoplasms | Antineoplastic Agents | Therapeutic Uses | Survival Analysis

Korea, Republic of
Terns, Inc.

Not yet recruiting

CARDINAL- A Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Efficacy of TERN-701 in Participants With Chronic Myeloid Leukemia

Chronic Myeloid Leukemia | Chronic Myeloid Leukemia, Chronic Phase

United States
Terns, Inc.

Completed

DUET Study: A Clinical Study to Evaluate the Safety, Efficacy, Pharmacokinetics and Pharmacodynamics of Orally Administered TERN-501 as Monotherapy and in Combination With TERN-101 in Noncirrhotic Adults With Presumed Non-Alcoholic Steatohepatitis

NASH - Nonalcoholic Steatohepatitis

United States
Terns, Inc.

Completed

LIFT Study: A Safety, Tolerability, Efficacy, and Pharmacokinetics Study of TERN-101 in Subjects With Non-Cirrhotic Non-Alcoholic Steatohepatitis (NASH)

NASH - Nonalcoholic Steatohepatitis

United States
Michael Stevens

Recruiting

Changes in Brain Function Through Repeated Emotion Regulation Training

Depression

United States
9 Meters Biopharma, Inc.

Terminated

VIBRANT Study of Vurolenatide in Adult Patients With Short Bowel Syndrome.

Short Bowel Syndrome

United States

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