Dana-Farber Cancer Institute
Dana-Farber Cancer Institute sponsors 781 registered US clinical trials on ClinicalTrials.gov, 112 of them currently recruiting, and 449 completed. 15 of these trials are in Phase 3-4 (later-stage) and 492 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Breast Cancer, with 53 trials.
Trial Pipeline
781 total, page 14 of 16
Using Positron Emission Tomography to Evaluate the Effects of Bevacizumab on Intra-tumoral Pharmacokinetics of 5-fluorouracil in Metastatic Colorectal Cancer
NCT00165568
Intensive Chemotherapy and Rituximab in the Treatment of Burkitt Lymphoma
NCT00126191
Cetuximab and Vinorelbine in Elderly Subjects With Lung Cancer
NCT00165334
Laboratory-Treated Lymphocyte Infusion After Haploidentical Donor Stem Cell Transplant
NCT00376480
Hormone Suppression and Radiation Therapy for 6 Months With/Without Docetaxel for High Risk Prostate Cancer
NCT00116142
05-001: Treatment of Acute Lymphoblastic Leukemia in Children
NCT00400946
Computerized Assessment for Patients With Cancer
NCT00194493
Evaluation of the Effects of Chemotherapy on the Uptake and Retention of Carbon 11 Methionine in Prostate Cancer Patients
NCT00139204
Chemotherapy Followed by Zevalin for Relapsed Mantle Cell Lymphoma
NCT00119730
Mifepristone (RU-486) in Androgen Independent Prostate Cancer
NCT00140478
Study of Bevacizumab, Erlotinib, FOLFOX for Patients With Untreated Metastatic Colorectal Cancer
NCT00116506
Vaccine Trial for Clear Cell Sarcoma, Pediatric Renal Cell Carcinoma, Alveolar Soft Part Sarcoma and Children With Stage IV Melanoma
NCT00258687
Etoposide, Cyclophosphamide, Thalidomide, Celecoxib, and Fenofibrate in Relapsed or Progressive Cancer
NCT00357500
Bevacizumab in Combination With Temozolomide in Patients With Neuroendocrine Tumors
NCT00137774
The PediQUEST Study: Evaluation of Pediatric Quality of Life and Evaluation of Symptoms Technology
NCT01838564
Upstaging of ALH/LCIS Found on Core Biopsy Based on Subsequent Excisional Biopsy
NCT00146536
Study of Xyotax (CT-2103) in Patients With Metastatic Breast Cancer
NCT00148707
Docetaxel in Combination With Iressa in Previously Treated Patients With Pancreatic Cancer
NCT00137761
Title XELOX FOR SALIVARY GLAND CANCERS
NCT00101075
Capecitabine in Women With Operable Breast Cancer
NCT00148720
CC-5013 (Lenalidomide) and Rituximab in Waldenstrom's Macroglobulinemia
NCT00142168
Combination Chemotherapy and Radiation in Treating Patients With Stage III or IV Head and Neck Cancer (Paradigm Trial)
NCT00095875
Combination Chemotherapy, Radiation Therapy and Surgery for Esophageal Cancer
NCT00165490
Avastin and Taxotere for Esophagogastric Cancer
NCT00137813
Bortezomib in Combination With CC-5013 in Patients With Relapsed/Refractory Multiple Myeloma
NCT00153933
Preoperative Cisplatin in Early Stage Breast Cancer
NCT00148694
Study of Dynavax's 1018 ISS, Following Rituxan in Patients With B-Cell Follicular Lymphoma
NCT00251394
Capecitabine For Nasopharyngeal Cancer
NCT00095901
GM-CSF Vaccinations After Allogeneic Blood Stem Cell Transplantation in Patients With Advanced Myeloid Malignancies
NCT00426205
Fulvestrant in Premenopausal Women With Hormone Receptor-Positive Breast Cancer
NCT00146601
Effects of Tibilone on Bone Density, Menopause Symptoms and Breast Density in Women After Prophylactic Oophorectomy
NCT00165204
Monitoring of Erythroid Lineage Specific Chimerism Following Allogeneic Hematopoietic Transplantation for Thalassemia Major
NCT00480506
Pleurectomy/Decortication With Intraoperative Intrathoracic/Intraperitoneal Heated Cisplatin With Sodium Thiosulfate
NCT00165503
Allogeneic Stem Cell Transplantation Following Chemotherapy in Patients With Hemoglobinopathies
NCT00153985
Thalidomide, Celecoxib, and Combination Chemotherapy in Treating Patients With Relapsed or Refractory Malignant Glioma
NCT00047281
Docetaxel, Estramustine and Short Term Androgen Withdrawal for Patients With a Rising PSA After Local Treatment
NCT00165399
Bevacizumab (Avastin) and Erlotinib (Tarceva) in Previously Treated Mesothelioma
NCT00137826
Rituximab Therapy for Steroid-Refractory Chronic Graft Versus Host Disease
NCT00136396
Dosimetric Analysis of Vaginal Cuff Brachytherapy in Endometrial Carcinoma
NCT00165126
Extrapleural Pneumonectomy With Intraoperative Intrathoracic/Intraperitoneal Heated Cisplatin With Amifostine and Sodium Thiosulfate
NCT00165516
A Study of Docetaxel Plus Carboplatin in Patients With Hormone Refractory Prostate Cancer
NCT00134706
Fludarabine and Rituximab for the Treatment of Marginal Zone Non-Hodgkin's Lymphoma
NCT00117156
Bortezomib (Velcade) in Waldenstrom's Macroglobulinemia
NCT00142129
Protein Tyrosine Kinases (PTK) in Multiple Myeloma
NCT00165347
Talotrexin in Treating Patients With Advanced or Recurrent Solid Tumors
NCT00098514
Bortezomib (Velcade) in Patients With Untreated Multiple Myeloma
NCT00153920
Effects of Exercise Intervention on Insulin Levels in Breast Cancer Survivors
NCT00153894
Sirolimus With Tacrolimus for Graft-vs-Host Disease Prophylaxis After Un-Related Stem Cell Transplantation
NCT00144677
Vaccination With Autologous, Lethally Irradiated Melanoma Cells Engineered by Adenoviral Mediated Gene Transfer to Secrete Granulocyte-Macrophage Stimulating Factor (GMSF)
NCT00809588
Tarceva and Capecitabine for Pancreatic Cancer
NCT00125021
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 1 | 181 |
| Phase 2 | 311 |
| Phase 3 | 14 |
| Phase 4 | 1 |
Therapeutic Areas
What the Pipeline for Dana-Farber Cancer Institute Shows
According to the ClinicalTrials.gov registry, Dana-Farber Cancer Institute is linked to 781 US clinical trials across every stage of research activity. Of those, 112 studies are currently recruiting, about 14% of the sponsor's indexed portfolio, and 449 are already marked complete, representing roughly 57% of the total.
The phase mix for Dana-Farber Cancer Institute reports 15 late-stage studies (Phase 3 and Phase 4 combined) and 492 earlier-phase studies (Phase 1 and Phase 2).
The top therapeutic focus area indexed for Dana-Farber Cancer Institute is Breast Cancer with 53 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.