Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Moderate Risk

Score: 35/100

Failure Rate

10.0%

2 terminated/withdrawn out of 20 trials

Success Rate

88.9%

+2.4% vs industry average

Late-Stage Pipeline

25%

5 trials in Phase 3/4

Results Transparency

6%

1 of 16 completed trials have results

Key Signals

1 recruiting1 with results

Enrollment Performance

Analytics

N/A
10(50.0%)
Phase 4
3(15.0%)
Phase 2
3(15.0%)
Phase 3
2(10.0%)
Phase 1
2(10.0%)
20Total
N/A(10)
Phase 4(3)
Phase 2(3)
Phase 3(2)
+1 more

Activity Timeline

Global Presence

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Clinical Trials (20)

Showing 20 of 20 trials
NCT06924502Not ApplicableRecruiting

Testing the Protective and Caring Effect of a Water-in-oil Formulation in Patients Suffering From Urinary and/or Fecal Incontinence and Requiring Incontinence Care Products

Role: lead

NCT06244615Not ApplicableCompleted

Clinical Trial of a Mouth and Throat Rinse for the Treatment of Acute Sore Throat

Role: lead

NCT04159610Phase 2Withdrawn

Assessment of Safety, Tolerability and Efficacy of 1% GPB Cream Versus Qbrexza® (Glycopyrronium) Cloth 2.4% Under Maximum-Use Conditions in Subjects with Primary Axillary Hyperhidrosis

Role: lead

NCT05863104Phase 2Completed

Assessment of Safety, Tolerability, Systemic Exposure and Efficacy of GPB Cream in Adolescents With Severe Primary Hyperhidrosis

Role: lead

NCT03630107Not ApplicableCompleted

In-Use Test of a Cosmetic Product in Subjects With Chronically Itchy Scalp

Role: lead

NCT03477058Not ApplicableCompleted

In-Use Test With a Cosmetic Product to Treat Pruritus

Role: lead

NCT03658616Phase 3Completed

Assessment of Efficacy and Safety of Topical Administration of 1% Glycopyrronium Bromide (GPB) in Patients With Primary Axillary Hyperhidrosis and the Assessment of Long-term Efficacy and Safety of Topical Administration of 1% GPB Cream in Patients With Primary Axillary Hyperhidrosis.

Role: lead

NCT05211505Phase 4Completed

Investigation of Efficacy and Tolerability of WO 2707, a MoistCream Cremolum, in Postmenopausal Women Suffering From Symptoms of Vaginal Dryness

Role: lead

NCT04222647Phase 2Completed

Investigation of Efficacy and Tolerability of a Lactic Acid Containing Vaginal Suppository in Post-menopausal Women With VVA

Role: lead

NCT04538183Not ApplicableCompleted

Use Test: Dermowas Body Lotion pH 4 vs. pH 5.8

Role: lead

NCT03037788Phase 1Completed

Investigation of Ascending Concentrations of Glycopyrronium Bromide (GPB) in a Topical Formulation in Subjects With Axillary Hyperhidrosis

Role: lead

NCT03629405Not ApplicableCompleted

Assessment of the Efficacy and Barrier Protection of Two Cosmetic Products

Role: lead

NCT03593122Not ApplicableCompleted

Investigation on the Efficacy of WO 2085 Moisturising Cream for Breast Cancer Patients Suffering From Vulvovaginal Dryness

Role: lead

NCT02269826Not ApplicableCompleted

Efficacy and Safety of Non-hormonal Vaginal Preparations in Treating Vaginal Dryness

Role: lead

NCT03252730Not ApplicableCompleted

In-Use Test With a Cosmetic Product

Role: lead

NCT03044652Phase 4Completed

Investigation of Non-inferiority of Treatment of Vulvovaginal Dryness With WO2085 Moisturising Cream in Comparison to a Cream With 0.1% Estriol

Role: lead

NCT01030666Phase 4Terminated

Effect of Postsurgical Systemic Doxycycline After Regenerative Periodontal Therapy

Role: collaborator

NCT02687789Not ApplicableCompleted

Safety, Tolerability and Efficacy of Vaginal Suppository WO3191 in the Post-treatment of Bacterial Vaginosis

Role: lead

NCT02576093Phase 1Completed

Safety, Tolerability, Pharmacokinetics and Efficacy of WOL071-007 in Atopic Dermatitis Patients

Role: lead

NCT00204269Phase 3Unknown

Three-Year Trial on a New Testosterone Gel

Role: collaborator

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