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WASHINGTON UNIVERSITY SCHOOL OF MEDICINE

WASHINGTON UNIVERSITY SCHOOL OF MEDICINE logo
πŸ‡ΊπŸ‡ΈUnited States
Ownership
Private, Subsidiary
Established
1891-01-01
Employees
10K
Market Cap
-
Website
http://www.medschool.wustl.edu

Clinical Trials

1.7k

Active:108
Completed:965

Trial Phases

6 Phases

Early Phase 1:64
Phase 1:286
Phase 2:258
+3 more phases

Drug Approvals

2

FDA:2

Drug Approvals

Fludeoxyglucose F 18

Approval Date
Oct 29, 2021
FDA

Ammonia N 13

Approval Date
Oct 29, 2021
FDA

Clinical Trials

Distribution across different clinical trial phases (1428 trials with phase data)β€’ Click on a phase to view related trials

Not Applicable
714 (50.0%)
Phase 1
286 (20.0%)
Phase 2
258 (18.1%)
Early Phase 1
64 (4.5%)
Phase 4
64 (4.5%)
Phase 3
42 (2.9%)

A Digital Intervention to Decrease Self-Stigma Among Pregnant and Postpartum Women With Substance Use Disorder

Not Applicable
Recruiting
Conditions
Substance Use Disorder
First Posted Date
2025-10-08
Last Posted Date
2025-10-08
Lead Sponsor
Washington University School of Medicine
Target Recruit Count
152
Registration Number
NCT07211867
Locations
πŸ‡ΊπŸ‡Έ

Washington University School of Medicine, St Louis, Missouri, United States

Recombinant Human IL-7 (NT-I7) in Relapsed/Refractory Multiple Myeloma Following BCMA CAR-T Therapy (Cilta-cel)

Not Applicable
Not yet recruiting
Conditions
Multiple Myeloma
Multiple Myeloma in Relapse
Multiple Myeloma, Refractory
Interventions
Drug: Placebo
Biological: B-cell Maturation Antigen (BCMA) CART-T therapy
First Posted Date
2025-09-30
Last Posted Date
2025-09-30
Lead Sponsor
Washington University School of Medicine
Target Recruit Count
40
Registration Number
NCT07200089
Locations
πŸ‡ΊπŸ‡Έ

Washington University School of Medicine, St Louis, Missouri, United States

Selinexor Maintenance Post CAR-T Cell Therapy for Multiple Myeloma

Not Applicable
Not yet recruiting
Conditions
Multiple Myeloma
Interventions
First Posted Date
2025-09-30
Last Posted Date
2025-09-30
Lead Sponsor
Washington University School of Medicine
Target Recruit Count
20
Registration Number
NCT07200102
Locations
πŸ‡ΊπŸ‡Έ

Washington University School of Medicine, St Louis, Missouri, United States

Efavirenz (EFV) Intensification

Not Applicable
Completed
Conditions
HIV
Interventions
First Posted Date
2025-09-26
Last Posted Date
2025-09-26
Lead Sponsor
Washington University School of Medicine
Target Recruit Count
7
Registration Number
NCT07193875
Locations
πŸ‡ΊπŸ‡Έ

Washington University in St Louis, St Louis, Missouri, United States

Multicontext Approach for Cognitive Function in Parkinson Disease

Not Applicable
Not yet recruiting
Conditions
PARKINSON DISEASE (Disorder)
First Posted Date
2025-09-24
Last Posted Date
2025-09-24
Lead Sponsor
Washington University School of Medicine
Target Recruit Count
114
Registration Number
NCT07190404
Locations
πŸ‡ΊπŸ‡Έ

Washington University School of Medicine, St Louis, Missouri, United States

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News

Eisai's Tau Antibody Etalanetug Receives FDA Fast Track Designation for Alzheimer's Disease

Eisai's investigational anti-MTBR tau antibody etalanetug (E2814) has been granted FDA Fast Track designation to expedite development for Alzheimer's disease treatment.

Reprieve Cardiovascular Secures $61 Million Series B Funding, Initiates Pivotal Heart Failure Trial

Reprieve Cardiovascular closed an oversubscribed $61 million Series B financing led by Deerfield Management to advance its intelligent decongestion management therapy for acute decompensated heart failure.

Universal CAR-T Cell Therapy Achieves 91% Response Rate in Aggressive T Cell Cancers

An international Phase I/II trial of WU-CART-007, a universal CAR-T cell therapy, demonstrated a 91% overall response rate in patients with relapsed or refractory T cell acute lymphoblastic leukemia and T cell lymphoblastic lymphoma.

FDA-Approved Alzheimer's Drug Lecanemab Shows Manageable Safety Profile in Real-World Setting

WashU Medicine researchers found only 1% of Alzheimer's patients treated with lecanemab experienced severe side effects requiring hospitalization, confirming clinical trial safety data in a real-world setting.

Immunotherapy Breakthrough: Pembrolizumab Doubles Disease-Free Survival in Locally Advanced Head and Neck Cancer

An international Phase 3 trial shows pembrolizumab (Keytruda) added to standard therapy extends disease-free survival from 30 to 51.8 months in patients with locally advanced head and neck cancer.

Heavy Cannabis Use Linked to Triple Mortality Risk and Rising Psychosis Cases, Studies Find

People diagnosed with cannabis use disorder (CUD) face nearly triple the risk of death over five years compared to the general population, with a tenfold increase in suicide risk, according to a large Canadian study.

AI Advances in Breast Cancer Detection: New Technologies Show Promise for Earlier Diagnosis

AI technology developed at Washington University can analyze sequential mammograms to identify subtle tissue changes, predicting breast cancer risk 2.3 times more accurately than standard methods.

Nutrition's Critical Role in Cancer Care: From Prevention to Survivorship

Nutrition plays a vital role throughout the cancer journey, with different dietary strategies needed during active treatment versus survivorship and prevention phases.

Wren Laboratories Launches Advanced NETest 2.0 for Enhanced Neuroendocrine Tumor Diagnostics

Wren Laboratories has introduced NETest 2.0, an AI-enhanced liquid biopsy test featuring a 51-gene mRNA expression algorithm, achieving over 95% sensitivity in NET detection and 90% accuracy in identifying disease progression.

Early Leqembi Patient's Journey Highlights Promise and Limitations of New Alzheimer's Treatment

β€’ One of the first U.S. patients to receive Leqembi (lecanemab) in 2020, Sue Bell's four-year treatment journey provides insights into the drug's real-world impact on Alzheimer's progression. β€’ While Leqembi successfully clears beta-amyloid plaques and can slow disease progression, the $25,000-per-year treatment shows varying effectiveness among patients and does not restore lost cognitive function. β€’ After four years of twice-monthly infusions, Sue Bell discontinued treatment as her condition progressed beyond the early stage where Leqembi provides optimal benefit.

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