Seagen

84 total trials 56 completed

Seagen sponsors 84 registered US clinical trials on ClinicalTrials.gov, none currently recruiting, and 56 completed. 3 of these trials are in Phase 3-4 (later-stage) and 81 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Lymphoma, Large B-Cell, Diffuse, with 2 trials.

Trial Pipeline

84 total, page 2 of 2

TERMINATED Phase 1

A Phase 1b Study of SGN-75 in Combination With Everolimus in Patients With Renal Cell Carcinoma

NCT01677390

COMPLETED Phase 2

Brentuximab Vedotin in Patients With CD30-positive Nonlymphomatous Malignancies

NCT01461538

COMPLETED Phase 2

A Study of Brentuximab Vedotin in Relapsed or Refractory Non-Hodgkin Lymphoma

NCT01421667

COMPLETED Phase 1

A Phase 1 Study of Brentuximab Vedotin Given Sequentially and Combined With Multi-Agent Chemotherapy for CD30-Positive Mature T-Cell and NK-Cell Neoplasms

NCT01309789

COMPLETED Phase 1

A Phase 1 Dose Escalation Trial of ASG-5ME in Pancreatic or Gastric Adenocarcinoma

NCT01166490

COMPLETED Phase 3

A Phase 3 Study of Brentuximab Vedotin (SGN-35) in Patients at High Risk of Residual Hodgkin Lymphoma Following Stem Cell Transplant (The AETHERA Trial)

NCT01100502

COMPLETED Phase 1

A Phase 1 Study of Brentuximab Vedotin Combined With Multi-Agent Chemotherapy for Hodgkin Lymphoma

NCT01060904

COMPLETED Phase 1

Cardiac Safety Study of Brentuximab Vedotin (SGN-35)

NCT01026233

COMPLETED Phase 1

Clinical Pharmacology Study of Brentuximab Vedotin (SGN-35)

NCT01026415

COMPLETED Phase 1

A Phase 1 Dose-escalation Trial of SGN-75 in CD70-positive Non-Hodgkin Lymphoma or Renal Cell Carcinoma

NCT01015911

COMPLETED Phase 2

A Brentuximab Vedotin Trial for Patients Who Have Previously Participated in a Brentuximab Vedotin Study

NCT00947856

COMPLETED Phase 2

A Phase 2 Open Label Trial of Brentuximab Vedotin (SGN-35) for Systemic Anaplastic Large Cell Lymphoma

NCT00866047

COMPLETED Phase 2

A Pivotal Open-Label Trial of Brentuximab Vedotin for Hodgkin Lymphoma

NCT00848926

COMPLETED Phase 1

A Study of ARRY-380 in Patients With Advanced HER2+ Cancer

NCT00650572

COMPLETED Phase 1

Trial to Define the Safety and Tolerability of SGN-40, Rituximab, and Gemcitabine in Patients With DLBCL

NCT00655837

COMPLETED Phase 1

A Phase I Study of Lintuzumab Combined With Lenalidomide in Patients With Myelodysplastic Syndromes (MDS)

NCT00502112

TERMINATED Phase 1

A Phase I Dose Escalation Study of SGN-35 Alone and in Combination With Gemcitabine for CD30-Positive Malignancies

NCT00649584

COMPLETED Phase 2

A Study of Lintuzumab (SGN-33) in Combination With Low Dose Cytarabine in Patients 60+ Years With AML

NCT00528333

TERMINATED Phase 2

A Randomized Phase IIb Placebo-Controlled Study of R-ICE Chemotherapy With and Without SGN-40 for Patients With DLBCL

NCT00529503

COMPLETED Phase 1

Study of SGN-40, Lenalidomide, and Dexamethasone in Patients With Multiple Myeloma

NCT00525447

COMPLETED Phase 2

Study of SGN-40 in Patients With Relapsed Diffuse Large B-Cell Lymphoma

NCT00435916

COMPLETED Phase 1

Phase I Open-Label Dose Finding Study of SGN-35 for CD30 Positive Hematologic Malignancies

NCT00430846

COMPLETED Phase 1

A Safety Study of Lintuzumab in Patients With Acute Myeloid Leukemia and Myelodysplastic Syndrome

NCT00283114

COMPLETED Phase 1

A Safety Study in Patients With Chronic Lymphocytic Leukemia

NCT00283101

COMPLETED Phase 1

A Safety Study of SGN-40 in Patients With Non-Hodgkin's Lymphoma

NCT00103779

COMPLETED Phase 2

Study of SGN-30 (Anti-CD30 mAb) in Patients With Primary Cutaneous Anaplastic Large Cell Lymphoma

NCT00099255

COMPLETED Phase 2

FDG-PET to Investigate SGN-15 and Docetaxel in Patients With Advanced Non-Small Cell Lung Carcinoma

NCT00086333

COMPLETED Phase 1

Study of SGN-40 in Patients With Refractory or Recurrent Multiple Myeloma

NCT00079716

COMPLETED Phase 2

Study of SGN-30 (Antibody) in Patients With Refractory or Recurrent Anaplastic Large Cell Lymphoma

NCT00079755

COMPLETED Phase 2

Study of SGN-15, Antibody-Drug Conjugate, to Treat Hormone Refractory Prostate Cancer

NCT00031187

TERMINATED Phase 2

Monoclonal Antibody Therapy and Docetaxel in Treating Women With Metastatic or Recurrent Breast Cancer

NCT00028483

COMPLETED Phase 2

Safety/Efficacy Study of Immunoconjugate With Docetaxel in Non-small Cell Lung Carcinoma

NCT00051571

COMPLETED Phase 1

A Safety/Efficacy Study of SGN-30 (Antibody) in Patients With Refractory or Recurrent CD30+ Hematologic Malignancies

NCT00051597

TERMINATED Phase 2

Safety/Efficacy Study of SGN-15 (Antibody-Drug Conjugate) Combined With Gemcitabine in Patients With Ovarian Cancer

NCT00051584

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What the Pipeline for Seagen Shows

According to the ClinicalTrials.gov registry, Seagen is linked to 84 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 56 are already marked complete, representing roughly 67% of the total.

The phase mix for Seagen reports 3 late-stage studies (Phase 3 and Phase 4 combined) and 81 earlier-phase studies (Phase 1 and Phase 2).

The top therapeutic focus area indexed for Seagen is Lymphoma, Large B-Cell, Diffuse with 2 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.