| Principal Investigator: |
|
Stephen Bartlett, M.D. |
| Source: |
|
Federal Grant |
| Clinical Trial Description: |
|
"Solid Organ Transplantation in HIV Positive Patients" |
| |
|
|
|
| Principal Investigator: |
|
Benjamin Philosophe, M.D., Ph.D. |
| Source: |
|
Novartis |
| Clinical Trial Description: |
|
"Predictors of Allograft Outcomes Relating to Optimal
Induction and Immunosuppressive Regimens for Populations at High Immunological
Risk for Poorer Allograft Outcomes" |
|
| |
|
|
| Principal Investigator: |
|
Luis Campos, M.D. |
| Source: |
|
Wyeth |
| Clinical Trial Description: |
|
"A Randomized, Open-Label, Comparative Evaluation
of Conversion From Calcineurin Inhibitor Treatment to Sirolimus Treatment
Versus Continued Calcineurin Inhibitor Treatment in Liver Allograft
Recipients Undergoing Maintenance Therapy" |
|
| |
|
|
| Principal Investigator: |
|
Matthew Cooper, M.D. |
| Source: |
|
Novartis |
| Clinical Trial Description: |
|
"A Six-Month, Prospective, Multi Center, Open Label,
Parallel, Randomized Study of The Safety, Tolerability and Efficacy
of Myfortic (Erl080) With Simulect, Corticosteroids, and Two Different
Levels of Tacrolimus in De Novo Renal Transplant Recipients (Cerl080a2409)" |
|
| |
|
|
| Principal Investigator: |
|
Matthew Cooper, M.D. |
| Source: |
|
Novartis |
| Clinical Trial Description: |
|
"A 24-Month, Multi-Center, Randomized, Open-Label
Non-Inferiority Study of The Efficacy and Safety Comparing Two Concentration-Controlled
Certican Regimens with Reduced Neoral Versus Myfortic with Standard
Dose Neoral in De Novo Renal Transplant Recipients" |
|
| |
|
|
| Principal Investigator: |
|
Matthew Cooper, M.D. |
| Source: |
|
Novartis |
| Clinical Trial Description: |
|
"A 4-Week, Multi Center, Double-Blind, Randomized,
Parallel Group Study to Compare the Gastrointestinal (GI) Safety and
Tolerability of Myfortic and Cellcept when Administered in Combination
with Calcineurin Inhibitors (CNI) in Renal Transplant Recipients Experiencing
Gastrointestinal Intolerance" |
| |
|
|
|
| Principal Investigator: |
|
Stephen Bartlett, M.D., Kristi Silver, M.D. |
| Source: |
|
|
| Clinical Trial Description: |
|
"Human Islet Transplantation in Non-Uremic Type
1 Diabetic Patients with Normal Native Renal Function" |
|
| |
|
|
| Principal Investigator: |
|
Matthew Cooper, M.D. |
| Source: |
|
|
| Clinical Trial Description: |
|
"Living Donation and Laparoscopic Nephrectomy" |
|
| |
|
|
| Principal Investigator: |
|
Stephen Bartlett, M.D. |
| Source: |
|
Department of Defense/Naval Grant |
| Clinical Trial Description: |
|
"A Study of the Safety and Efficacy of the Use of
Islet Cell Transplantation in Patients with Type 1 Diabetes" |
|
| |
|
|
| Principal Investigator: |
|
Matthew Cooper, M.D. |
| Source: |
|
|
| Clinical Trial Description: |
|
"Blood-Type Incompatible Live Donor Kidney Transplantation" |