Solvay Pharmaceuticals
Solvay Pharmaceuticals sponsors 35 registered US clinical trials on ClinicalTrials.gov, none currently recruiting, and 29 completed. 19 of these trials are in Phase 3-4 (later-stage) and 15 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Highly Active Antiretroviral Therapy (HAART)-Related Nausea and Vomiting, with 1 trials.
Trial Pipeline
35 total, page 1 of 1
Study of Serum Testosterone Levels in Non-dosed Females After Secondary Exposure
NCT00998933
Study Investigating a Delayed-Release Pancrelipase in Patients With Pancreatic Exocrine Insufficiency Due to Cystic Fibrosis
NCT00775528
Safety and Efficacy Study to Evaluate the Effect of SLV320 on Renal Function in Patients With Worsening Heart Failure
NCT00744341
Study Investigating a Delayed-Release Pancrelipase in Patients With Pancreatic Exocrine Insufficiency (PEI) Due to Cystic Fibrosis (CF)
NCT00690820
Study Investigating a Delayed-Release Pancrelipase in Patients With Exocrine Pancreatic Insufficiency Due to Cystic Fibrosis
NCT00510484
A Study to Investigate the Effect of Delayed Release Pancrelipase on Maldigestion in Patients With Exocrine Pancreatic Insufficiency Due to Chronic Pancreatitis and Pancreatectomy
NCT00414908
Study to Evaluate the Effect of SLV320 in Addition to Chronic Furosemide Treatment on Renal Function in Subjects With Congestive Heart Failure and Impaired Renal Function
NCT00568009
An Open Label SLV308 Safety Extension to Study S308.3.003 in Early PD Patients
NCT00335374
An Open Label SLV308 Safety Extension to Study S308.3.002 in Patients With Parkinson's Disease Experiencing Motor Fluctuations.
NCT00407095
Compare the Effects of Bifeprunox and Quetiapine on Weight Changes in Stable Schizophrenic Patients
NCT00396214
SLV308 for Treatment of Patients With Parkinson's Disease Experiencing Motor Fluctuations
NCT00406588
An Open Label SLV308 Safety Extension to Study S308.3.001 in Early PD Patients
NCT00332917
Switch Study of Existing Atypical Antipsychotics to Bifeprunox
NCT00347425
SLV 308 and Pramipexole for Treatment of Patients With Early Parkinson Disease
NCT00335166
SLV308 for Treatment of Patients With Early Parkinson's Disease
NCT00269516
Progressively Decreasing Titration Schedules of Bifeprunox in Subjects With Schizophrenia or Bipolar Disorder
NCT00139919
Treatment of Elderly Subjects With Psychosis and Behavioral Disturbances Associated With Dementia of the Alzheimer's Type
NCT00160147
Study to Evaluate the Efficacy and Safety of Dronabinol Metered Dose Inhaler (MDI) in Acute Treatment of Migraine Headache
NCT00123201
Twice Daily Titration Study of Bifeprunox in Subjects With Schizophrenia
NCT00139906
Comparison of Estrogen and Methyltestosterone Combination Treatments for Postmenopausal Hot Flushes
NCT00160342
To Evaluate the Impact of Treatment Interruption on Re-initiation of Bifeprunox
NCT00141479
PK Effects of Bifeprunox & Valproate in Bipolar I
NCT00141505
Intravenous Tedisamil in the Rapid Conversion of Atrial Fibrillation or Flutter to Normal Sinus Rhythm in Female Subjects
NCT00126022
Safety and Efficacy of PROMETRIUM® Capsules in Induction of Secretory Conversion
NCT00160199
Intravenous Tedisamil in the Rapid Conversion of Atrial Fibrillation or Flutter to Normal Sinus Rhythm in Male Subjects
NCT00126061
Efficacy and Safety of Androgel in the Treatment of Hypogonadal and Low Testosterone Men With Type 2 Diabetes
NCT00141492
Intravenous Tedisamil in the Rapid Conversion of Atrial Fibrillation or Flutter to Normal Sinus Rhythm in Female Subjects
NCT00126074
The Efficacy of ESTRATEST® Tablets in Relieving Menopausal Symptoms in Estrogenized, Hysterectomized Postmenopausal Women
NCT00141557
The Efficacy of ESTRATEST® Tablets in Relieving Menopausal Symptoms in Estrogenized, Non-Hysterectomized Postmenopausal Women
NCT00141544
Study of the Efficacy of ESTRATEST® H.S. Tablets in Relieving Menopausal Symptoms in Estrogenized Postmenopausal Women
NCT00141570
Dronabinol Versus Placebo in Treatment and Prevention of Highly Active Anti-Retroviral Therapy (HAART)-Related Nausea and Vomiting
NCT00642499
Dronabinol Versus Standard Ondansetron Antiemetic Therapy in Preventing Delayed-Onset Chemotherapy-Induced Nausea and Vomiting
NCT00642512
Observation Study of T-Gel (1%) in Treatment of Adolescent Boys With Hypogonadism
NCT00193661
Pharmacokinetic Evaluation of Testosterone Gel (1%)
NCT00193700
Efficacy of Pancrelipase on Postprandial Belching and Bloating.
NCT00266721
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 1 | 2 |
| Phase 2 | 13 |
| Phase 3 | 18 |
| Phase 4 | 1 |
What the Pipeline for Solvay Pharmaceuticals Shows
According to the ClinicalTrials.gov registry, Solvay Pharmaceuticals is linked to 35 US clinical trials across every stage of research activity. Of those, 0 studies are currently recruiting, about 0% of the sponsor's indexed portfolio, and 29 are already marked complete, representing roughly 83% of the total.
The phase mix for Solvay Pharmaceuticals reports 19 late-stage studies (Phase 3 and Phase 4 combined) and 15 earlier-phase studies (Phase 1 and Phase 2).
The top therapeutic focus area indexed for Solvay Pharmaceuticals is Highly Active Antiretroviral Therapy (HAART)-Related Nausea and Vomiting with 1 linked trial, and 6 other condition areas appear in the top list above.
How to read these pipeline numbers
Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.
A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work, safety, dosing, and early signal detection, and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.
That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice, verify current details directly with ClinicalTrials.gov before relying on any figure here.
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page aggregates every registered trial from this sponsor, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.