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Stanford University

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Stanford, California 94305
Global Leader in Type 1 Diabetes
Global Leader in Depression
Conducts research for Cancer
Conducts research for Diabetes
Conducts research for Premature Birth
1398 reported clinical trials
207 medical researchers
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Summary

Stanford University is a medical facility located in Stanford, California. This center is recognized for care of Type 1 Diabetes, Depression, Cancer, Diabetes, Premature Birth and other specialties. Stanford University is involved with conducting 1,398 clinical trials across 1,687 conditions. There are 207 research doctors associated with this hospital, such as Andrei Iagaru, MD, Robert Lowsky, MD, Christopher Chen, and Antonio Hardan, MD.

Area of expertise

1Type 1 Diabetes
Global Leader
Stanford University has run 98 trials for Type 1 Diabetes. Some of their research focus areas include:
mIAA positive
IA-2A positive
ICA positive
2Depression
Global Leader
Stanford University has run 66 trials for Depression.

Top PIs

Clinical Trials running at Stanford University

Ovarian Cancer
Lazy Eye
Atrial Fibrillation
Follicular Lymphoma
Mantle Cell Lymphoma
Cystic Fibrosis
Carcinoid Tumor
Fuchs' Dystrophy
Fallopian Tube Cancer
Neuroendocrine Tumors
Image of trial facility.

Heated Chemotherapy + Niraparib

for Ovarian Cancer

Patients will be registered prior to, during or at the completion of neoadjuvant chemotherapy (Paclitaxel 175 mg/m2 IV over 3 hours and Carboplatin AUC 6 IV on Day 1 every 21 days for 3-4 cycles). Registered patients who progress during neoadjuvant chemotherapy will not be eligible for iCRS and will be removed from the study. Following completion of neoadjuvant chemotherapy, interval cytoreductive surgery (iCRS) will be performed in the usual fashion in both arms. Patients will be randomized at the time of iCRS (iCRS must achieve no gross residual disease or no disease \>1.0 cm in largest diameter) to receive HIPEC or no HIPEC. Patients randomized to HIPEC (Arm A) will receive a single dose of cisplatin (100mg/m2 IP over 90 minutes at 42 C) as HIPEC. After postoperative recovery patients will receive standard post-operative platinum-based combination chemotherapy. Patients randomized to surgery only (Arm B) will receive postoperative standard chemotherapy after recovery from surgery. Both groups will receive an additional 2-3 cycles of platinum-based combination chemotherapy per institutional standard (Paclitaxel 175 mg/m2 IV over 3 hours and Carboplatin AUC 6 IV on Day 1 every 21 days for 2-3 cycles) for a maximum total of 6 cycles of chemotherapy (neoadjuvant plus post-operative cycles) followed by niraparib individualized dosing until progression or 36 months (if no evidence of disease).
Recruiting2 awards Phase 3
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Mirvetuximab + Bevacizumab

for Ovarian Cancer

GLORIOSA is a Phase 3 multicenter, open label study designed to evaluate the safety and efficacy of mirvetuximab Soravtansine + Bevacizumab as maintenance therapy in participants with platinum-sensitive ovarian, primary peritoneal or fallopian tube cancers with high folate receptor-alpha (FRα) expression.
Recruiting2 awards Phase 3
Image of trial facility.

B7-H3 CAR T Cells

for Ovarian Cancer

This is a single site, open label, Phase 1 study using a 3 + 3 dose escalation design in two cohorts of adults with recurrent, platinum-resistant ovarian tumors.
Recruiting1 award Phase 15 criteria

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Unbiased ResultsWe believe in providing patients with all the options.
Your Data Stays Your DataWe only share your information with the clinical trials you're trying to access.
Verified Trials OnlyAll of our trials are run by licensed doctors, researchers, and healthcare companies.
Terms of Service·Privacy Policy·Cookies·Security
Unbiased ResultsWe believe in providing patients with all the options.
Your Data Stays Your DataWe only share your information with the clinical trials you're trying to access.
Verified Trials OnlyAll of our trials are run by licensed doctors, researchers, and healthcare companies.
Terms of Service·Privacy Policy·Cookies·Security