Forest Laboratories

145 total trials 127 completed

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 2 of 3

COMPLETED Phase 2

Safety and Efficacy of Levomilnacipran ER (F2695 SR) in Adults With Fatigue Associated With Major Depressive Disorder

NCT01254305

TERMINATED Phase 2

Long-Term Safety and Efficacy Study of Milnacipran in Pediatric Patients With Primary Fibromyalgia

NCT01331109

COMPLETED Phase 2

Comparative Study of Coadministered Ceftaroline Fosamil and NXL104 vs. Intravenous Doripenem in Adult Subjects With Complicated Urinary Tract Infections

NCT01281462

COMPLETED Phase 4

Efficacy and Safety Study to Evaluate Combination Therapy With Nebivolol and Lisinopril vs. Placebo and Monotherapy in Patients With Stage 2 Diastolic Hypertension

NCT01218100

COMPLETED Phase 4

Safety Study of Escitalopram in Children 7 to 11 Years of Age With Major Depressive Disorder

NCT01198795

TERMINATED Phase 1

A Study of EUR-1066 in Subjects With Chronic Pancreatitis, Exocrine Pancreatic Insufficiency and Chronic Abdominal Pain

NCT01159119

COMPLETED Phase 4

PR-018: An Open-Label, Safety Extension of Study PR-011

NCT01131507

COMPLETED Phase 4

A Study to Evaluate the Mode of Administration and Safety of EUR-1008 (APT-1008) in Infants 1 to 12 Months of Age

NCT01100606

COMPLETED Phase 3

Long-term Study of Cariprazine in Patients With Schizophrenia

NCT01104792

COMPLETED Phase 3

Safety and Efficacy of Cariprazine in Schizophrenia

NCT01104779

COMPLETED Phase 3

Safety and Efficacy of Cariprazine in Patients With Schizophrenia

NCT01104766

COMPLETED Phase 3

Relapse-Prevention Study With Levomilnacipran ER (F2695 SR) in Patients With Major Depressive Disorder

NCT01085812

COMPLETED Phase 4

Nebivolol in Patients With Systolic Stage 2 Hypertension

NCT01057251

TERMINATED Phase 3

Safety and Efficacy of Dutogliptin in Patients With Type 2 Diabetes Mellitus Receiving Background Treatment With Glimepiride Alone or in Combination With Metformin or With Pioglitazone Alone

NCT01089790

COMPLETED Phase 3

Long-term Safety and Tolerability of Cariprazine for Bipolar I Disorder

NCT01059539

COMPLETED Phase 3

Safety and Efficacy of Cariprazine for Bipolar I Disorder

NCT01058668

COMPLETED Phase 4

Study of Milnacipran in Patients With Inadequate Response to Duloxetine for the Treatment of Fibromyalgia

NCT01077375

COMPLETED Phase 3

Safety and Efficacy of Cariprazine for Mania

NCT01058096

COMPLETED Phase 3

Safety Study of F2695 SR in Major Depressive Disorder

NCT01034267

COMPLETED Phase 3

Safety and Efficacy of Levomilnacipran ER (F2695 SR) in Major Depressive Disorder

NCT01034462

TERMINATED Phase 3

Efficacy and Safety Study of MAX-002 Suppository Versus Placebo and Active Medicine in Mild to Moderate Ulcerative Proctitis

NCT01016262

COMPLETED Phase 2

Open-label Study of Safety and Tolerability of Memantine in Children With Autism

NCT01999894

COMPLETED Phase 4

Discontinuation Study of the Durability of Effect of Milnacipran for the Treatment of Fibromyalgia

NCT01014585

TERMINATED Phase 3

Study of the Safety and Efficacy of Apadenoson for Detection of Myocardial Perfusion Defects Using SPECT MPI

NCT00990327

COMPLETED Phase 3

Safety and Efficacy of Levomilnacipran ER (F2695 SR) in Major Depressive Disorder

NCT00969709

COMPLETED Phase 3

Safety and Efficacy of Levomilnacipran ER (F2695 SR) in Major Depressive Disorder

NCT00969150

TERMINATED Phase 3

Safety and Efficacy of Dutogliptin in Patients With Type 2 Diabetes Mellitus (T2DM) on Background Therapy With Pioglitazone

NCT00970424

COMPLETED Phase 3

Trial of Linaclotide Administered to Patients With Irritable Bowel Syndrome With Constipation

NCT00948818

TERMINATED Phase 3

Safety and Efficacy of Dutogliptin in Patients With Type 2 Diabetes Mellitus (T2DM) on Background Therapy With Glimepiride With or Without Metformin

NCT00947557

COMPLETED Phase 2

Safety and Efficacy of RGH-188 (Cariprazine) in Bipolar Depression

NCT00852202

COMPLETED Phase 2

Safety and Efficacy of Cariprazine As Adjunctive Therapy In Major Depressive Disorder

NCT00854100

COMPLETED Phase 2

A Study of Cariprazine in Patients With Chronic Stable Schizophrenia

NCT00839852

COMPLETED Phase 2

Study of Pharmacokinetics, Safety, Efficacy, and Tolerability of Memantine in Children With Autism

NCT00872898

COMPLETED Phase 3

Use of Ultrase® MT12 in Young Cystic Fibrosis Children (CF)

NCT00880100

COMPLETED Phase 2

Study of the Safety and Efficacy of RGH-896 in Patients With Diabetic Peripheral Neuropathic Pain

NCT00838799

COMPLETED Phase 3

Study of Milnacipran Added to Pregabalin for Treatment of Fibromyalgia

NCT00797797

COMPLETED Phase 4

A Study on the Long-term Efficacy of Nebivolol After Withdrawal of Therapy

NCT00785512

TERMINATED Phase 3

Effect of Milnacipran on Pain Processing and Functional Magnetic Resonance Imaging (fMRI) Activation Patterns in Patients With Fibromyalgia

NCT00793520

COMPLETED Phase 3

An Open-Label, Long-Term Safety Study of Linaclotide in Patients With Chronic Constipation or Irritable Bowel Syndrome With Constipation

NCT00765999

COMPLETED Phase 3

Phase III, Randomized, Double-Blind, Placebo-Controlled, Trial of Linaclotide Administered to Patients With Chronic Constipation

NCT00765882

COMPLETED Phase 4

A Study on the Efficacy and Safety of Nebivolol Monotherapy in Hispanic Hypertensive Patients

NCT00770861

COMPLETED Phase 4

Efficacy and Safety of Nebivolol (Added to Lisinopril or Losartan) in Hypertensive Patients

NCT00734630

COMPLETED Phase 4

Study of the Glycemic Effects of Nebivolol Compared With Metoprolol and HCTZ in Diabetic Hypertensive Patients

NCT00744237

COMPLETED Phase 2

Safety and Efficacy of Cariprazine (RGH-188) in the Acute Exacerbation of Schizophrenia

NCT00694707

COMPLETED Phase 4

The Blood Pressure and Metabolic Effects of Nebivolol in Hypertensive Patients With Impaired Glucose Tolerance or Impaired Fasting Glucose

NCT00673790

COMPLETED Phase 2

Study To Assess Efficacy and Safety of Oglemilast in Patients With Chronic Obstructive Pulmonary Disease (COPD)

NCT00671073

COMPLETED Phase 4

The Effect of Nebivolol in Hypertensive Patients With Coronary Artery Disease

NCT00673075

COMPLETED Phase 3

Escitalopram in Adult Patients With Major Depressive Disorder

NCT00668525

COMPLETED Phase 3

Randomized, Double-Blind, Placebo Controlled Study of Vilazodone's Efficacy, Safety, and Biomarkers of Response in Major Depressive Disorder (MDD)

NCT00683592

COMPLETED Phase 1

Pharmacokinetics of Ceftaroline in Subjects 12 to 17 Years of Age

NCT00633126

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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.

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.