| Name of study |
Indication |
Description |
Patients |
Status |
IBS-D |
Irritable Bowel Syndrome with Diarrhoea |
Double-blind, randomised, placebo-controlled, parallel group study to evaluate the effect of a 4-week treatment, 1, 3 or 10mg/d oral treatment Ibodutant vs. Placebo.
|
18 -70 years
|
Currently recruiting patients |
| Colitis ulcerosa |
Mild to moderate distal Colitis Ulcerosa |
2-week randomised, double-blind, placebo-controlled, clinical parallel group study with increasing doses to evaluate safety, agree-ableness of a new natural drug, rectal treatment in the evening. |
18 – 75 years |
Currently recruiting patients |
| Acute Knee Injury |
Acute cartilage injury of knee within the past 4 to 12 weeks |
Clinical research study to test the safety and effectiveness of an experimental drug, placebo-controlled, i.a. injection, MRT to measure the injury. |
18 – 45 years |
Currently recruiting patients |
| Chronic Unspecified Back Pain |
Back pain for at least
3 months, in rest and movement, without basic cause |
Local treatment of an approved medication, placebo-controlled. |
18 – 75 years |
Currently recruiting patients |
| Constipation |
Patients with moderate to severe pain and constipation due to daily therapy with strong analgesic |
Parallel-group, double-blind, placebo-controlled study to approve a new strong analgesic.
|
18 years and above |
Currently recruiting patients |
| Vaccination against Zoster |
Prophylaxis to avoid Herpes Zoster |
Approved Vaccine against Herpes Zoster, i.m. or subcutaneous vaccination, no placebo. |
40 years and above |
Currently recruiting patients |
| COPD |
Smoker and Ex-Smoker with COPD |
A 24-week, randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of a new inhalation powder and the individual components once-daily in subjects with known Chronic Obstructive Pulmonary Disease. |
40 years and above |
Currently recruiting patients |
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| Chronic Idiopathic Urticaria |
Chronic Idiopathic Urticaria, symptomatic despite antihistamine treatment (H1) |
A Phase III, multicenter, randomized, double-blind, dose-ranging, placebo-controlled study to evaluate the efficacy, response duration and safety of Xolair® (Omalizumab) in patients with Chronic Idiopathic Urticaria (CIU) who remain symptomatic despite antihistamine treatment (H1/H2). |
12 - 75 years |
Soon recruiting patients |
| Hypertension |
Essential Hypertension
Grade 2/ 3, under treatment with 1 – 3 agents |
A Phase-3 randomized, double-blind, efficacy and safety study evaluating the fixed dose
combinations of a new drug plus Chlorthalidone (40/12.5 mg and 40/25 mg) in patients who do not achieve target blood pressure following treatment of the 40 mg Monotherapy. |
18 years and above |
Soon recruiting patients |
| Depression |
Primary Major Depression |
Multicenter, randomized, double-blind, double-dummy, flexible-dose, placebo-controlled parallel study in the relapse prevention of stabilized patients, in remission, with MDD. |
18 years and above |
Soon recruiting patients |
| Hypersensitivity to Grass Pollen |
Hypersensitivity to Grass Pollen with or without intermittent Asthma. |
Randomized, double-blind, parallel group, multicenter study to evaluate the efficacy and safety of four doses of Depigoid® Phleum in Patients with allergic rhinitis and/or rhino-conjunctivitis with or without intermittent asthma. No placebo. |
18 -70 years |
Soon recruiting patients |
| Psoriasis |
Plaque-type Psoriasis |
Phase 2 multicenter, randomized, placebo-controlled dose-ranging trial evaluating the efficacy and safety of a new Biological in the treatment of subjects with moderate to severe Plaque-type Psoriasis. |
18 years and above |
Soon recuiting patients |
| Name of study |
Indication |
Description |
Patients |
Status |