CEDARS-SINAI MEDICAL CENTER
- Country
- 🇺🇸United States
- Ownership
- Private, Subsidiary
- Established
- 1902-01-01
- Employees
- 12K
- Market Cap
- -
- Website
- http://www.cedars-sinai.org
Clinical Trials
420
Trial Phases
6 Phases
Drug Approvals
0
Drug Approvals
No drug approvals found
This company may not have drug approvals in our database
Clinical Trials
Distribution across different clinical trial phases (317 trials with phase data)• Click on a phase to view related trials
Functional Outcomes in Ulcerative Colitis Patients With Ileal Pouch Anal Anastomosis Treated With High Intensity Focused Electromagnetic Stimulation
- Conditions
- Fecal Incontinence
- First Posted Date
- 2025-06-24
- Last Posted Date
- 2025-06-24
- Lead Sponsor
- Cedars-Sinai Medical Center
- Target Recruit Count
- 20
- Registration Number
- NCT07034443
- Locations
- 🇺🇸
Cedars Sinai Medical Center, Los Angeles, California, United States
Phase II Trial of Ivonescimab in Combination With Carboplatin + Docetaxel in Patients With Early-Stage Triple Negative Breast Cancer
- Conditions
- TNBCTNBC - Triple-Negative Breast CancerEarly Stage Triple-Negative Breast Carcinoma
- Interventions
- First Posted Date
- 2025-06-12
- Last Posted Date
- 2025-06-12
- Lead Sponsor
- Cedars-Sinai Medical Center
- Target Recruit Count
- 34
- Registration Number
- NCT07017673
- Locations
- 🇺🇸
Cedars-Sinai Medical Center, Los Angeles, California, United States
🇺🇸Cedars-Sinai Medical Center Beverly Hills, Los Angeles, California, United States
🇺🇸Huntington Cancer Center, an Affiliate of CS Cancer, Pasadena, California, United States
Small Intestinal Bacterial Overgrowth (SIBO) in Pancreatic Adenocarcinoma (PDAC)
- Conditions
- Pancreatic AdenocarcinomaWeight Loss
- First Posted Date
- 2025-05-23
- Last Posted Date
- 2025-05-23
- Lead Sponsor
- Cedars-Sinai Medical Center
- Target Recruit Count
- 100
- Registration Number
- NCT06988150
- Locations
- 🇺🇸
Cedars-Sinai Medical Center, Los Angeles, California, United States
This Study is to Evaluate Whether Receiving Education and Glucose Monitoring With the CGM Device Will Improve Patient-reported Outcomes by Improving Patient's Satisfaction and Quality of Life (QOL) With Glucose Monitoring Device.
- Conditions
- Diabetes Mellitus
- First Posted Date
- 2025-05-11
- Last Posted Date
- 2025-05-11
- Lead Sponsor
- Cedars-Sinai Medical Center
- Target Recruit Count
- 37
- Registration Number
- NCT06965803
Ostomy Readmission Reduction Program
- Conditions
- Ostomy - Ileostomy or Colostomy
- First Posted Date
- 2025-05-04
- Last Posted Date
- 2025-05-04
- Lead Sponsor
- Cedars-Sinai Medical Center
- Target Recruit Count
- 40
- Registration Number
- NCT06956274
- Locations
- 🇺🇸
Surgery Group LA, Los Angeles, California, United States
- Prev
- 1
- 2
- 3
- 4
- 5
- 84
- Next
News
Percheron Therapeutics Acquires Phase II-Ready Anti-VISTA Cancer Immunotherapy HMBD-002 in $290M Deal
Percheron Therapeutics has licensed HMBD-002, a first-in-class monoclonal antibody targeting the VISTA immune checkpoint, from Hummingbird Bioscience in a deal worth up to $290 million.
Studies Reveal Concerning Trends in Prostate Cancer Treatment: Overtreatment Rising Despite Serious Long-Term Risks
Recent research shows increasing overtreatment of prostate cancer in older men with limited life expectancy, with radiation therapy use rising from 16% to 39% despite guidelines recommending against such interventions.
Trodelvy-Keytruda Combination Shows Promising Results in First-Line Treatment for Triple-Negative Breast Cancer
Gilead Sciences and Merck's phase 3 ASCENT-04/KEYNOTE-D19 trial demonstrated statistically significant improvement in progression-free survival with Trodelvy plus Keytruda compared to Keytruda with chemotherapy in metastatic TNBC patients.
Hospital-Based Addiction Consultation Significantly Improves OUD Treatment Outcomes, Study Shows
A clinical trial found that hospital-based addiction consultation services more than doubled the rate of medication initiation for opioid use disorder during hospitalization (57.3% vs 26.7% with usual care).
ABVC BioPharma Projects $19 Million Revenue from Global Licensing Deals and Strategic CDMO Acquisition
ABVC BioPharma has secured three global licensing agreements valued at $959 million across psychiatric disorders, ophthalmology, and oncology, expecting to generate approximately $19 million in cash revenue in 2025.
FDA-Approved Itovebi Combination for Advanced Breast Cancer Requires Careful Blood Sugar Monitoring
The FDA has approved Itovebi in combination with Ibrance and Faslodex for PIK3CA-mutated, HR-positive, HER2-negative advanced breast cancer, based on the INAVO120 trial results.
AHA Advisory: EVT Shows Promise in Large-Core Stroke Treatment, Six Clinical Trials Reveal
Recent data from six randomized controlled trials involving 1,887 patients demonstrates significant benefits of endovascular therapy (EVT) in large-core stroke patients, with functional independence rates of 19.5% versus 7.9% for medical management alone.
Cardiac Surgeons Call for Greater Role as Transcatheter Tricuspid Valve Treatments Advance
Recent FDA approvals of transcatheter tricuspid valve devices, including Evoque and TriClip, are transforming treatment options for tricuspid regurgitation patients who historically avoided surgery.
Antibody-Drug Conjugates Offer New Hope in Breast Cancer Treatment
• Antibody-drug conjugates (ADCs) represent a promising class of targeted therapies in breast cancer, delivering chemotherapy directly to cancer cells. • Clinical trials are exploring over 150 ADCs, including LCB84, showing potential in patients with heavily pre-treated or resistant cancers. • ADCs like Enhertu and Trodelvy have demonstrated significant efficacy, even in tumors with low target expression, shifting paradigms in treatment. • Researchers emphasize the importance of understanding the distinct side effect profiles of different ADCs for optimal patient management.
Heart Failure Trial Endpoints: Balancing Cause-Specific and All-Cause Outcomes
A meta-analysis of 113 heart failure (HF) trials reveals that all-cause hospitalization (ACH) is reported in approximately half of the trials, with no significant improvement over time.