Solvay Pharmaceuticals

35 total trials 29 completed

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

COMPLETED Phase 1

Study of Serum Testosterone Levels in Non-dosed Females After Secondary Exposure

NCT00998933

COMPLETED Phase 3

Study Investigating a Delayed-Release Pancrelipase in Patients With Pancreatic Exocrine Insufficiency Due to Cystic Fibrosis

NCT00775528

TERMINATED Phase 2

Safety and Efficacy Study to Evaluate the Effect of SLV320 on Renal Function in Patients With Worsening Heart Failure

NCT00744341

COMPLETED Phase 3

Study Investigating a Delayed-Release Pancrelipase in Patients With Pancreatic Exocrine Insufficiency (PEI) Due to Cystic Fibrosis (CF)

NCT00690820

COMPLETED Phase 3

Study Investigating a Delayed-Release Pancrelipase in Patients With Exocrine Pancreatic Insufficiency Due to Cystic Fibrosis

NCT00510484

COMPLETED Phase 3

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

TERMINATED

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

COMPLETED Phase 3

An Open Label SLV308 Safety Extension to Study S308.3.003 in Early PD Patients

NCT00335374

COMPLETED Phase 3

An Open Label SLV308 Safety Extension to Study S308.3.002 in Patients With Parkinson's Disease Experiencing Motor Fluctuations.

NCT00407095

TERMINATED Phase 3

Compare the Effects of Bifeprunox and Quetiapine on Weight Changes in Stable Schizophrenic Patients

NCT00396214

COMPLETED Phase 3

SLV308 for Treatment of Patients With Parkinson's Disease Experiencing Motor Fluctuations

NCT00406588

COMPLETED Phase 3

An Open Label SLV308 Safety Extension to Study S308.3.001 in Early PD Patients

NCT00332917

COMPLETED Phase 3

Switch Study of Existing Atypical Antipsychotics to Bifeprunox

NCT00347425

COMPLETED Phase 3

SLV 308 and Pramipexole for Treatment of Patients With Early Parkinson Disease

NCT00335166

COMPLETED Phase 3

SLV308 for Treatment of Patients With Early Parkinson's Disease

NCT00269516

COMPLETED Phase 2

Progressively Decreasing Titration Schedules of Bifeprunox in Subjects With Schizophrenia or Bipolar Disorder

NCT00139919

TERMINATED Phase 3

Treatment of Elderly Subjects With Psychosis and Behavioral Disturbances Associated With Dementia of the Alzheimer's Type

NCT00160147

COMPLETED Phase 2

Study to Evaluate the Efficacy and Safety of Dronabinol Metered Dose Inhaler (MDI) in Acute Treatment of Migraine Headache

NCT00123201

COMPLETED Phase 2

Twice Daily Titration Study of Bifeprunox in Subjects With Schizophrenia

NCT00139906

COMPLETED Phase 2

Comparison of Estrogen and Methyltestosterone Combination Treatments for Postmenopausal Hot Flushes

NCT00160342

COMPLETED Phase 2

To Evaluate the Impact of Treatment Interruption on Re-initiation of Bifeprunox

NCT00141479

COMPLETED Phase 2

PK Effects of Bifeprunox & Valproate in Bipolar I

NCT00141505

COMPLETED Phase 3

Intravenous Tedisamil in the Rapid Conversion of Atrial Fibrillation or Flutter to Normal Sinus Rhythm in Female Subjects

NCT00126022

COMPLETED Phase 4

Safety and Efficacy of PROMETRIUM® Capsules in Induction of Secretory Conversion

NCT00160199

COMPLETED Phase 3

Intravenous Tedisamil in the Rapid Conversion of Atrial Fibrillation or Flutter to Normal Sinus Rhythm in Male Subjects

NCT00126061

COMPLETED Phase 2

Efficacy and Safety of Androgel in the Treatment of Hypogonadal and Low Testosterone Men With Type 2 Diabetes

NCT00141492

COMPLETED Phase 3

Intravenous Tedisamil in the Rapid Conversion of Atrial Fibrillation or Flutter to Normal Sinus Rhythm in Female Subjects

NCT00126074

TERMINATED Phase 2

The Efficacy of ESTRATEST® Tablets in Relieving Menopausal Symptoms in Estrogenized, Hysterectomized Postmenopausal Women

NCT00141557

TERMINATED Phase 2

The Efficacy of ESTRATEST® Tablets in Relieving Menopausal Symptoms in Estrogenized, Non-Hysterectomized Postmenopausal Women

NCT00141544

COMPLETED Phase 2

Study of the Efficacy of ESTRATEST® H.S. Tablets in Relieving Menopausal Symptoms in Estrogenized Postmenopausal Women

NCT00141570

COMPLETED Phase 2

Dronabinol Versus Placebo in Treatment and Prevention of Highly Active Anti-Retroviral Therapy (HAART)-Related Nausea and Vomiting

NCT00642499

COMPLETED Phase 3

Dronabinol Versus Standard Ondansetron Antiemetic Therapy in Preventing Delayed-Onset Chemotherapy-Induced Nausea and Vomiting

NCT00642512

COMPLETED Phase 2

Observation Study of T-Gel (1%) in Treatment of Adolescent Boys With Hypogonadism

NCT00193661

COMPLETED Phase 1

Pharmacokinetic Evaluation of Testosterone Gel (1%)

NCT00193700

COMPLETED Phase 3

Efficacy of Pancrelipase on Postprandial Belching and Bloating.

NCT00266721

Phase Distribution

PhaseTrial 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.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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.