Forest Laboratories
Forest Laboratories sponsors 145 registered US clinical trials on ClinicalTrials.gov, none currently recruiting, and 127 completed. 100 of these trials are in Phase 3-4 (later-stage) and 43 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Major Depressive Disorder, with 9 trials.
Trial Pipeline
145 total, page 3 of 3
Efficacy and Safety of Ceftaroline Versus Linezolid in Subjects With Complicated Skin and Skin Structure Infections
NCT00633152
A Randomized, Double-Blind, Dose Response-Control, Crossover Study to Evaluate the Safety and Efficacy of Two Doses of EUR-1008 (APT-1008) in Chronic Pancreatitis (CP) Participants With Exocrine Pancreatic Insufficiency (EPI)
NCT00788593
Comparative Study of Ceftaroline vs. Ceftriaxone in Adult Subjects With Community-Acquired Pneumonia
NCT00621504
A One Year Open Label Study Assessing the Safety and Tolerability of Vilazodone in Patients With Major Depressive Disorder (MDD)
NCT00644358
Safety and Efficacy Study of Viokase® 16 for the Correction of Steatorrhea
NCT00559364
A Study of the Effect of Nebivolol to Evaluate Its Vasodilatory Effects in Hypertensive Patients
NCT00648895
Study to Evaluate Symptoms in Patients Treated With Nebivolol or Metoprolol Extended-release (ER) for Hypertension
NCT00547300
A Study Of Milnacipran In Patients With Fibromyalgia: Effects On 24 Hour Ambulatory Blood Pressure Monitoring
NCT00618956
Efficacy and Safety of Ultrase® MT20 in Improving the Coefficient of Fat Absorption (CFA) in Children With Cystic Fibrosis (CF) and Pancreatic Insufficiency (PI)
NCT00513682
Comparative Study of Ceftaroline vs. Ceftriaxone in Adults With Community-Acquired Pneumonia
NCT00509106
Study Evaluating Cariprazine (RGH-188) in the Treatment of Patients With Acute Mania
NCT00488618
Comparative Study of Ceftaroline vs. Vancomycin Plus Aztreonam in Adult Subjects With Complicated Skin Infections
NCT00423657
Comparative Study of Ceftaroline vs. Vancomycin Plus Aztreonam in Adult Subjects With Complicated Skin Infections
NCT00424190
Study Evaluating RGH-188 in the Treatment of Patients With Schizophrenia
NCT00404573
Safety and Efficacy Study of ULTRASE® MT20 in Participants With Cystic Fibrosis (CF) and Exocrine Pancreatic Insufficiency (PI)
NCT00408317
Fixed Dose Comparison of Escitalopram to an Active Comparator in Severely Depressed Patients
NCT00384436
Acamprosate Initiated During Alcohol Detoxification
NCT00360594
Efficacy and Safety of Itopride vs Placebo in Heartburn
NCT00382577
A Comparison Study of Apadenoson and Adenosine to Treadmill Exercise Stress.
NCT00380198
Study of Oglemilast for the Prevention of Asthma.
NCT00322283
The Safety and Efficacy of Dexloxiglumide for the Relief of Symptoms of Functional Dyspepsia.
NCT00303264
Study of Oglemilast for the Treatment of Asthma
NCT00322686
Study to Evaluate the Safety and Efficacy of EUR-1008 (APT-1008) Pancreatic Enzyme Product in Participants With Cystic Fibrosis and Exocrine Pancreatic Insufficiency
NCT00297167
Study of Pancreatic Enzyme Product in Pediatric Participants With Cystic Fibrosis and Exocrine Pancreatic Insufficiency
NCT00981214
Study of Milnacipran for the Treatment of Fibromyalgia
NCT00314249
Effect of Azimilide Dihydrochloride on Renal Function
NCT00318838
Compassionate Use Study of 125 mg Per Day of Azimilide Dihydrochloride in One Patient
NCT00752596
Effects of Itopride on Gastric Motor and Sensory Functions in Healthy Volunteers
NCT00370110
Study of Memantine in Assessment of Selected Measures of Volumetric Magnetic Resonance Imaging (MRI) and Cognition in Moderate AD (Alzheimer's Disease)
NCT00334906
A Phase II Optimization Study of BMS068645 and Sestamibi Planar Imaging
NCT00162071
A Study of the Safety and Efficacy of Memantine in Moderate to Severe Alzheimer's Disease
NCT00322153
Study of Desmoteplase (International Nonproprietary Name [INN]) in Acute Ischemic Stroke (DIAS-2)
NCT00111852
A Study to Examine MPI SPECT Imaging With BMS068645 and Adenosine Compared to Coronary Angiography
NCT00162084
Comparison of Escitalopram Combination in Adult Patients With Major Depressive Disorder
NCT00109044
Study of Escitalopram in Adult Patients With Major Depressive Disorder
NCT00108979
The Safety and Efficacy of Escitalopram in Pediatric Patients With Major Depressive Disorder
NCT00107120
An Evaluation of the Safety and Efficacy of Memantine in Patients With Acute Mania Associated With Bipolar I Disorder
NCT00106405
Study of Milnacipran for the Treatment of Fibromyalgia
NCT00098124
An Evaluation of the Safety and Efficacy of Memantine in Agitated Patients With Moderate to Severe Alzheimer's Disease
NCT00097916
Evaluation of the Safety and Efficacy of Memantine as Adjunctive Treatment in Schizophrenia Patients
NCT00097942
The Safety and Efficacy of Neramexane in Patients With Moderate to Severe Alzheimer's Disease
NCT00090116
Long Term Safety of 125 mg Per Day of Oral Azimilide in Patients With Implantable Cardioverter Defibrillator (ICDs)
NCT00751738
Efficacy and Safety Evaluation of Azimilide Dihydrochloride in Patients With Implantable Cardioverter Defibrillators
NCT00035490
Efficacy and Safety of Azimilide in the Prophylactic Treatment of Patients With Atrial Fibrillation.
NCT00035464
Efficacy and Safety of Azimilide for the Treatment of Patients With Atrial Fibrillation
NCT00035477
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 1 | 9 |
| Phase 2 | 34 |
| Phase 3 | 75 |
| Phase 4 | 25 |
What the Pipeline for Forest Laboratories Shows
According to the ClinicalTrials.gov registry, Forest Laboratories is linked to 145 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 127 are already marked complete, representing roughly 88% of the total.
The phase mix for Forest Laboratories reports 100 late-stage studies (Phase 3 and Phase 4 combined) and 43 earlier-phase studies (Phase 1 and Phase 2).
The top therapeutic focus area indexed for Forest Laboratories is Major Depressive Disorder with 9 linked trials, and 9 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.