Masonic Cancer Center, University of Minnesota
Masonic Cancer Center, University of Minnesota sponsors 249 registered US clinical trials on ClinicalTrials.gov, 36 of them currently recruiting, and 127 completed. 1 of these trials are in Phase 3-4 (later-stage) and 183 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Acute Myeloid Leukemia, with 7 trials.
Trial Pipeline
249 total, page 2 of 5
Ruxolitinib, Human Chorionic Gonadotropin (uhCG/EGF), and Dose De-escalated Corticosteroids
NCT05123040
MT2021-27 FT538 Recurrent Ovarian, Fallopian Tube, and Primary Peritoneal Cancer
NCT05708924
EMR Chemotoxicity Risk Calculator To Decrease Chemotherapy Toxicity
NCT05809557
QuitGuide for American Indians: Aims 2 & 3
NCT05447156
App-Assisted Day Reconstruction to Reduce Logistic Toxicity in Cancer
NCT05502302
HCW9218 in Select Advanced Solid Tumors
NCT05322408
PTCy + Sirolimus/VIC-1911 as GVHD Prophylaxis in Myeloablative PBSC Transplantation
NCT05120570
Sugars in Cigarettes
NCT05308316
FT538 in Combination With Daratumumab in AML Acute Myeloid Leukemia
NCT04714372
Telehealth-Filter Ventilation ( COMET2P1 )
NCT04969783
Study of Periodontitis and Blood Stream Infection in AML Patients Receiving Chemotherapy
NCT04858594
Impact of Low Nicotine Cigarette Messaging on Perceptions and Cigarette Choices
NCT04740008
FT516 and IL2 With Enoblituzumab for Ovarian Cancer
NCT04630769
Clinical Trial of Two Study Drinks in Detoxification of Environmental Toxicants and Carcinogens
NCT03978117
FT596 With Rituximab as Relapse Prevention After Autologous HSCT for NHL
NCT04555811
Metabolism of NNK in Japanese Americans
NCT04228952
Multiple Dosing of Mesenchymal Stromal Cells in Patients With ARDS (COVID-19)
NCT04466098
Study of FT516 for the Treatment of COVID-19 in Hospitalized Patients With Hypoxia
NCT04363346
Multi-Ctr PII Cmb.Modality Tx Ruxolitinib, Decitabine, and DLI for Post HSCT in AML/MDS
NCT04055844
A Pilot Feasibility Study of Activated Charcoal in Healthy Volunteers
NCT04204772
A Study of FMT in Patients With AML Allo HSCT in Recipients
NCT03678493
Assessment of Complete Pathologic Response After Neoadjuvant Chemotherapy for Breast Cancer
NCT03981705
Radiation and Combination Immunotherapy for Melanoma
NCT03850691
Trial of Indole-3-Carbinol and Silibinin
NCT03687073
CMV-MVA Triplex Vac.Enhance Adap. NK Cell Recon. After Auto HSCT in pt Lymphoid Malig
NCT03383055
COMET2 Project 1 Filter Ventilation Study
NCT03637972
Exemestane in Post-Menopausal Women With NSCLC
NCT02666105
Monitoring of Immune and Microbial Reconstitution in (HCT) and Novel Immunotherapies
NCT03557749
Improving Self-Efficacy, Resolving Inflammaging Allo HSCT Survivors in Personal Training
NCT03609203
Nivolumab and Oral Cyclophosphamide for R/R AML and HIgh Risk MDS
NCT03417154
Haploidentical Allogeneic Hematopoietic Stem Cell Transplantation (HaploHCT) Following Reduced Intensity Conditioning (RIC) for Selected High Risk Non-Malignant Diseases
NCT03367546
BLASST-1 (Bladder Cancer Signal Seeking Trial): Nivolumab, Gemcitabine, and Cisplatin in Treatment of Muscle Invasive Bladder Cancer (MIBC) Undergoing Cystectomy
NCT03294304
Microbiota Changes in Acute Myeloid Leukemia Patients Undergoing Intensive Chemotherapy
NCT03728699
Physical Rehabilitation Evaluation and Optimal Physical Therapy (PRE-OPT)
NCT04225572
Intraperitoneal Delivery of Adaptive Natural Killer (NK) Cells (FATE-NK100) With Intraperitoneal Int
NCT03213964
Ph I Trial of NAM NK Cells and IL-2 for Adult Pts With MM and NHL
NCT03019666
IP ALT-803 Followed by SQ ALT-803 for Ovarian Cancer
NCT03054909
Gut Microbiota in Intestinal Barrier Damage in Acute Leukemia Patients Undergoing Inpatient Induction
NCT03316456
QUILT-3.033: Haplo NK With SQ ALT-803 for Adults With Relapsed or Refractory AML
NCT03050216
UCB Transplant for Hematological Diseases Using a Non Myeloablative Prep
NCT02722668
Open Label NK Cell Infusion (FATE-NK100) With Subq IL-2 in Adults With AML
NCT03081780
Relapse Prophylaxis With N-803 for AML and MDS Pts Following Allo HSCT
NCT02989844
Study of Brentuximab Vedotin And Bevacizumab In Refractory CD-30 Positive Germ Cell Tumors
NCT02988843
Allo HSCT Using RIC for Hematological Diseases
NCT02661035
Adoptive TReg Cell for Suppression of aGVHD After UCB HSCT for Heme Malignancies
NCT02991898
Reduced Intensity (RIC) Conditioning And Transplantation of HLA-Haplo-HCT
NCT02988466
Glucobrassicin-Brussel Sprout Effect on D10 Phe Metabolism
NCT02999399
Study of Cellutome System for Treatment of Individual Lesions in EB Pts
NCT02670837
Study of Pregnyl as Adjunct Therapy for High-Risk or Refractory Acute GVHD
NCT02525029
MT2015-20: Biochemical Correction of Severe EB by Allo HSCT and Serial Donor MSCs
NCT02582775
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 1 | 76 |
| Phase 2 | 107 |
| Phase 3 | 1 |
What the Pipeline for Masonic Cancer Center, University of Minnesota Shows
According to the ClinicalTrials.gov registry, Masonic Cancer Center, University of Minnesota is linked to 249 US clinical trials across every stage of research activity. Of those, 36 studies are currently recruiting, about 14% of the sponsor's indexed portfolio, and 127 are already marked complete, representing roughly 51% of the total.
The phase mix for Masonic Cancer Center, University of Minnesota reports 1 late-stage studies (Phase 3 and Phase 4 combined) and 183 earlier-phase studies (Phase 1 and Phase 2).
The top therapeutic focus area indexed for Masonic Cancer Center, University of Minnesota is Acute Myeloid Leukemia with 7 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.