AbbVie (prior sponsor, Abbott)

Closed portfolio with an early-phase archive tilt

According to ClinicalTrials.gov-derived indexes, AbbVie (prior sponsor, Abbott) sits in the top decile of US sponsors by registered trial count (#265 of 15,742 sponsors by registered trial count).

88 total trials none currently recruiting 83 completed early-phase tilt top decile by trial count

AbbVie (prior sponsor, Abbott): 88 sponsored US clinical trials, none currently recruiting.

AbbVie (prior sponsor, Abbott) sponsors 88 registered US clinical trials on ClinicalTrials.gov, none currently recruiting, and 83 completed. 17 of these trials are in Phase 3-4 (later-stage) and 70 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Lupron, with 1 trials.

Top-decile sponsor footprint

AbbVie (prior sponsor, Abbott) ranks in the top decile of sponsors by registered trial count (#265 of 15,742 sponsors by registered trial count). Volume at this scale usually reflects a long institutional pipeline, read phase tilt and therapeutic areas below before treating it as current-year activity.

Trial completion reliability score

C 76/100

83 of 88 decided trials (Completed vs. Terminated on ClinicalTrials.gov) reached their planned completion (94.3%), vs. national p10 68.4% / p90 100% among 1,234 sponsors with at least 10 decided trials. Still-open trials (Recruiting, Active-not-recruiting, Not-yet-recruiting) are excluded since they have not reached an outcome yet.

Indexed trials (enrollment closed)

88 total, page 1 of 2

COMPLETED Phase 2

Study in Rheumatoid Arthritis for Subjects Who Completed Preceding Study M13-390 With Adalimumab

NCT01752855

COMPLETED Phase 1

A Study in Healthy Adults and Adult Subjects With Rheumatoid Arthritis to Evaluate the Safety, Tolerability and Pharmacokinetics After Multiple Doses of ABT-494

NCT01741493

COMPLETED Phase 1

A Study to Evaluate the Safety, Tolerability and Pharmacokinetics of ABT-199 in Female Patients With Systemic Lupus Erythematosus (SLE)

NCT01686555

COMPLETED Phase 1

A Study of ABT-414 in Subjects With Solid Tumors

NCT01741727

COMPLETED Phase 1

A Study to Evaluate the Safety, Tolerability and Pharmacokinetics of Multiple Subcutaneous Injections of ABT-981 in Patients With Osteoarthritis of the Knee

NCT01668511

TERMINATED Phase 2

Safety and Tolerability Study Evaluating a New Treatment for Subjects With Mild to Moderate Alzheimer's Disease

NCT01690195

COMPLETED Phase 2

A Phase 2 Study to Evaluate ABT-126 for the Treatment of Cognitive Deficits in Schizophrenia

NCT01678755

TERMINATED Phase 2

This is a Safety and Tolerability Study Evaluating a New Treatment for Subjects With Mild to Moderate Alzheimer's Disease

NCT01676935

COMPLETED Phase 2

Open-label Extension Study of Navitoclax in Subjects With Chronic Lymphocytic Leukemia (CLL)

NCT01557777

COMPLETED Phase 1

A Clinical Study Conducted in Multiple Centers Evaluating Escalating Doses of Veliparib in Combination With Capecitabine and Radiation in Patients With Locally Advanced Rectal Cancer

NCT01589419

COMPLETED Phase 2

A Study in Rheumatoid Arthritis (RA) Patients to Compare Two Formulations of Adalimumab for Pharmacokinetic, Pharmacodynamic and Safety

NCT01712178

COMPLETED Phase 2

A Study to Evaluate ABT-126 for the Treatment of Cognitive Deficits in Schizophrenia

NCT01655680

TERMINATED Phase 2

A Study Comparing the Efficacy and Safety of ABT-652 to Placebo in Subjects With Diabetic Neuropathic Pain

NCT01579279

COMPLETED Phase 2

Evaluate the Efficacy and Safety of ABT-126 in Subjects With Mild to Moderate Alzheimer's Disease on Stable Doses of Acetylcholinesterase Inhibitors

NCT01549834

COMPLETED Phase 2

Evaluate the Efficacy and Safety of ABT-126 in Subjects With Mild to Moderate Alzheimer's Disease

NCT01527916

COMPLETED Phase 2

Study to Assess the Safety, Tolerability, Pharmacokinetics and Antiviral Activity of ABT-267 in HCV Infected Subjects

NCT01563536

TERMINATED Phase 2

Efficacy and Safety Study of ABT-436 in Major Depressive Disorder

NCT01741142

COMPLETED Phase 2

A Study of ABT-652 in Combination With a Nonsteroidal Anti-Inflammatory Drug (NSAID) in Adults With Osteoarthritis Pain of the Knee

NCT01444365

COMPLETED Phase 2

ABT-450 With Ritonavir and ABT-267 and/or ABT-333 With and Without Ribavirin in Genotype 1 Hepatitis C Virus Infected Patients

NCT01464827

COMPLETED Phase 1

An Extension Study of ABT-806 in Subjects With Advanced Solid Tumors

NCT01406119

COMPLETED Phase 2

A Prospective, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate Efficacy and Safety of Atrasentan, Including Thoracic Bioimpedance, in Type 2 Diabetic Subjects With Nephropathy

NCT01399580

COMPLETED Phase 1

An Open-label Study of the Effects of Elagolix in Adult Premenopausal Females

NCT01403038

COMPLETED Phase 2

Phase 2 Chronic Low Back Pain Study

NCT01364922

COMPLETED Phase 2

Evaluate the Efficacy and Safety of Once Daily Administration of Atrasentan Tablets (Low and High) Compared to Placebo in Reducing Residual Albuminuria in Type 2 Diabetic Patients With Nephropathy Who Are Treated With the Maximum Tolerated Labeled Dose of a Renin Angiotensin System (RAS) Inhibitor

NCT01356849

COMPLETED Phase 2

A Multicenter Study Comparing the Analgesic Effects and Safety of ABT-639 Compared to Placebo in Subjects With Diabetic Neuropathic Pain

NCT01345045

COMPLETED Phase 2

Acute Pain Study Following Bunionectomy

NCT01333722

COMPLETED Phase 2

Study of ABT-267 in Treatment Naive Hepatitis C Virus (HCV) Genotype 1 Infected Subjects

NCT01314261

COMPLETED Phase 2

A Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of ABT-450 With Ritonavir (ABT-450/r) When Given Together With ABT-333 and Ribavirin (RBV) in Treatment-Naïve and Non-responder Subjects With Genotype 1 Chronic Hepatitis C Virus (HCV) Infection

NCT01306617

COMPLETED Phase 1

A Study of ABT-806 in Subjects With Advanced Solid Tumor Types

NCT01255657

COMPLETED Phase 3

Study to Determine the Effects of Different Doses of Methotrexate (MTX) When Taken With Adalimumab in Subjects With Early Rheumatoid Arthritis (RA)

NCT01185301

COMPLETED Phase 2

A Pilot Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Antiviral Activity of ABT-450 With Ritonavir (ABT-450/r) Dosed in Combination With ABT-072 and Ribavirin (RBV)

NCT01221298

COMPLETED Phase 4

A Study to Determine the Effect of Methotrexate (MTX) Dose on Clinical Outcome and Ultrasonographic Signs in Subjects With Moderately to Severely Active Rheumatoid Arthritis (RA) Treated With Adalimumab (MUSICA)

NCT01185288

COMPLETED Phase 2

A Study of ABT-652 in Adults With Osteoarthritis Pain of the Knee

NCT01207115

TERMINATED

Study to Evaluate Safety of Vitamin D Receptor Activators in Patients Ages 0 to 16 With Chronic Kidney Disease Stage 5 Receiving Peritoneal Dialysis Within Current Clinical Practice

NCT01134315

COMPLETED Phase 2

The Usability and Injection Time of the Physiolis Syringe and Autoinjector in Rheumatoid Arthritis Patients

NCT01163617

COMPLETED Phase 1

ABT-348 as Monotherapy and in Combination With Azacitidine to Treat Advanced Hematologic Malignancies

NCT01110473

COMPLETED Phase 2

A Trial of ABT-888 in Combination With Temozolomide Versus Pegylated Liposomal Doxorubicin Alone in Ovarian Cancer

NCT01113957

COMPLETED Phase 2

Efficacy and Safety Study for Cognitive Deficits in Adult Subjects With Schizophrenia

NCT01077700

COMPLETED Phase 2

Safety and Efficacy Study for Cognitive Deficits in Adult Subjects With Schizophrenia

NCT01095562

COMPLETED Phase 1

Evaluating the Safety and Tolerability of the Poly-ADP Ribose (PARP) Inhibitor With FOLFIRI in Subjects With Solid Tumor

NCT01123876

COMPLETED Phase 1

ABT-348 as Monotherapy or Combination With Carboplatin or Docetaxel to Treat Advanced Solid Tumors

NCT01110486

COMPLETED Phase 2

A Randomized Study to Evaluate the Safety, Tolerability and Antiviral Activity of ABT-450, ABT-333 and ABT-072

NCT01074008

COMPLETED Phase 3

Study of Efficacy, Safety and Tolerability of Levodopa-Carbidopa Intestinal Gel in Levodopa-Responsive Parkinson's Subjects

NCT00660387

COMPLETED Phase 2

Hydrocodone/Acetaminophen for Acute Pain Following Bunionectomy

NCT01038609

COMPLETED Phase 1

Study of ABT-263 When Administered in Combination With Either Fludarabine/Cyclophosphamide/Rituximab or Bendamustine/Rituximab in Relapsed or Refractory Chronic Lymphocytic Leukemia

NCT00868413

COMPLETED Phase 2

Efficacy and Safety Study for Subjects With Mild-to-Moderate Alzheimer's Disease

NCT00948909

COMPLETED Phase 1

A Study Evaluating ABT-263 With Erlotinib, ABT-263 With Irinotecan, and ABT-263 Monotherapy in Cancer Subjects

NCT01009073

COMPLETED Phase 1

A Study Evaluating the Safety of ABT-263 in Combination With Etoposide/Cisplatin in Subjects With Cancer

NCT00878449

COMPLETED Phase 3

Study of Adalimumab in Patients With Axial Spondyloarthritis

NCT00939003

COMPLETED Phase 2

Hydrocodone/Acetaminophen for Acute Pain Following Third Molar Tooth Extraction

NCT00935311

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How the AbbVie (prior sponsor, Abbott) early-phase archive is shaped

88 indexed studies, none listed as recruiting (0% open); 83 completed (94%).

Phase mix: 17 late (III/IV) vs 70 early (I/II) (early-phase heavy).

Top condition: Lupron (1 trial), 9 others listed.

How to read a closed sponsor archive

When recruiting_count is zero, the indexed set is completed or otherwise not open. Phase tilt still describes where archived studies sat on the investigational pathway. Re-check ClinicalTrials.gov before acting.

AbbVie (prior sponsor, Abbott): archived-pipeline peers nationwide

Peers matched on 88 indexed studies with no current recruiting: volume and archive shape, not condition overlap.

AbbVie (prior sponsor, Abbott) sits at or above the median trial volume and at or above the median recruiting share among these 9 nationwide peers -- the two do not always move together. Source: ClinicalTrials.gov (2026-08-08 snapshot). 2×2 strategic matrix plotting 9 entities by Total trials (X) and Recruiting share (Y), with a crosshair dividing the plot into four quadrants. Higher volume & more openFocused & more openHigher volume, mostly closedSmaller & mostly closed 020406080100 0%5%10%15%20%25% Total trials Recruiting share AbbVie (prior sponsor, Abbott)Pacira PharmaceuticalsUniversity of Medicine and Dentistry of New JerseyAbbott NutritionFlorida International University10xBio22nd Century Group23andMe3-C Institute for Social Development
AbbVie (prior sponsor, Abbott) sits at or above the median trial volume and at or above the median recruiting share among these 9 nationwide peers -- the two do not always move together. Source: ClinicalTrials.gov (2026-08-08 snapshot).

AbbVie (prior sponsor, Abbott) sits at or above the median trial volume and at or above the median recruiting share among these 9 nationwide peers -- the two do not always move together.

Sponsors near 88 archived trials

Sponsors with similar archive density (± trial count)

What to do with this AbbVie (prior sponsor, Abbott) page

88 registered trials is a research-attention snapshot, not an endorsement of AbbVie (prior sponsor, Abbott) or any single study.

  • None of AbbVie (prior sponsor, Abbott)'s trials are currently recruiting in this registry; that can change as new trials post, or check the broader research index. Browse research indexes
  • Lupron is the condition AbbVie (prior sponsor, Abbott) studies most, compare against other sponsors active in the same condition before evaluating a specific study. See Lupron trials
  • Bring the specific trial ID (NCT number) to your own doctor before enrolling, this page is a directory, not medical guidance. Read the trial-finding guide

Trial and recruiting counts reflect ClinicalTrials.gov registry status as of the data vintage above; individual trial eligibility and enrollment status can change.

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. AbbVie (prior sponsor, Abbott) pipeline card: 88 registered trials from official public datasets. See our editorial standards & corrections policy, the methodology behind these numbers, the data changelog, or report a data error.