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HARESH S. JHANGIANI, M.D., F.A.C.P., M.B.A. CAREER MISSION STATEMENT To tender compassionate and exceptional quality healthcare to all my patients and provide the necessary leadership, knowledge, and skills to develop and maintain a comprehensive research program for the benefit of all cancer patients. PROFESSIONAL EXPERIENCE 2002 – Present COMPASSIONATE CANCER CARE MEDICAL GROUP, INC. 2002 – Present CORONA REGIONAL CANCER CENTER - Medical Director 1988 – 2002 PACIFIC COAST HEMATOLOGY/ONCOLOGY MEDICAL GROUP 1995 - 1999 FOUNTAIN VALLEY REGIONAL HOSPITAL AND MEDICAL CENTER MEDICAL LEADERSHIP POSITIONS Chairman, Working Tumor Board 2000-2003 HOSPITAL AFFILATION APPOINTMENTS Fountain Valley Regional Hospital and Medical Center CLINICAL RESEARCH ACTIVITY BLADDER CANCER A Randomized Phase III Study of Gemcitabine plus Cisplatin versus MVAC Chemotherapy in Advanced or Metastatic Transitional Cell Carcinoma of the Urothelium. Interleukin 2 in an Alternative Dose: Treatment of Patients with Metastatic Renal Cell Cancer with Low Dose Proleukin. BREAST CANCER Phase III trial of novel XXXXX plus capecitabine vs. capecitabine alone in patients with advanced breast cancer in previously treated with anthracycline and a taxine A Randomized, open-label phase III, study of RPR109881-IV vs. XXXXX in patients with metastatic breast cancer progressive after taxanes and anthracycline therapy A randomized, double-blind, parallel group, multicenter, phase III study comparing efficacy and tolerability of XXXXX 500 mg w/ XXXXX 250 mg in postmenopausal women with ER+ positive advanced breast cancer progressing or relapsing after previous therapy Randomized Trial of Gemcitabine Plus Docetaxel vs. Docetaxel Plus Capecitabine in Metastatic Breast Cancer in 1st and 2nd Line Patients An Open-Label, Randomized, Multicenter Study to Evaluate the Use of Zoledronic Acid in the Prevention of Cancer Treatment Related Bone Loss in Postmenopausal Women with ER+ and/or PR+ Breast Cancer Receiving Letrozole as Adjuvant Therapy A Double-Blind, Placebo-Controlled, Multicenter, Randomized Study Evaluating the Prophylactic Use of Pegfilgrastim on the Incidence of Febrile Neutropenia in Subjects with Advanced Breast Cancer Treated with Single Agent Docetaxel A Multicenter Phase III Randomized Trial Comparing Docetaxel In Combination With Doxorubicin And Cyclophosphamide (TAC) Versus Doxorubicin And Cyclophosphamide Followed By Docetaxel (ACT) As Adjuvant Treatment Of Operable Breast Cancer HER2NEU Negative Patients With Positive Auxiliary Lymph Nodes A Multicenter Phase III Randomized Trial Comparing Doxorubicin and Cyclophosphamide Followed by Docetaxel (ACT) with Doxorubicin and Cyclophosphamide Followed by Docetaxel and Trastuzumab (ACTH) and with Docetaxel, Platinum Salt and Trastuzumab (TCH) in the Adjuvant Treatment of Node Positive and High Risk Node Negative Patients with Operable Breast Cancer Containing the HER2NEU Alteration A Multicenter Phase III Randomized Trial Comparing Docetaxel (Taxotere®) and Trastuzumab (Herceptin®) with Docetaxel (Taxotere®), Carboplatin, and Trastuzumab (Herceptin®) as First line Chemotherapy for Patients with Advanced Breast Cancer Containing the HER2Gene Amplification Phase III Study Of Epirubicin/Cyclophosphamide Followed By Taxane (Sequential Chemotherapy) Versus Epirubicin/Taxane (Concurrent Chemotherapy) Adjuvant Treatment Operable, Node-Positive Breast Cancer Clinical Outcomes in Patients with HER2 Gene-Amplified Metastatic Breast Cancer Treated with First-Line Herceptin® in Combination with a Taxane: A Phase IV, Prospective, Community-Based Study The Traviota Study: Trastuzumab (Herceptin®) and Either Vinorelbine (Navelbine®) or Taxane-Based Chemotherapy in Patients with HER2 Overexpressing Metastatic Breast Cancer: A Randomized Phase III Study A Phase III Study of Doxorubicin-Cyclophosphamide Therapy Followed By Paclitaxel or Docetaxel Given Weekly Or Every 3 Weeks In Patients With Auxiliary Node-Positive Breast Cancer A Randomized Comparison of Medroxyprogesterone Acetate (MA) And Observation For Prevention Of Endometrial Pathology In Postmenopausal Breast Cancer Patients Treated With Tamoxifen A Multicenter, Open-Label, Randomized Study Of Three Schedules Of Weekly Taxol Induction Therapy Followed By Weekly Taxol Maintenance Therapy In Metastatic Breast Cancer Patients
An Epidemiologic Study Of Breast Cancer Risk Assessment Along With Breast Cancer Prevention And The Use Of Tamoxifen At The Center For Breast Care Of Orange County Regional Cancer At Fountain Valley Medical Center Beta Site For Tenet Health Care Comparison of CGS-16949A vs. Megestrol Acetate in Post-Menopausal Women With Breast Carcinoma. Daunoxome For The Treatment of Metastatic Breast Cancer (Phase II). A Comparative Trial of Droloxifene and Tamoxifen as First-line Hormonal Therapy in Women With Advanced Breast Cancer. Comparison of Two Doses (0.5mg. And 2.5mg) of Letrozole (CGS 20267) Versus Megestrol Acetate in Postmenopausal Women With Advanced Breast Cancer. Aredia (Pamidronate Disodium) Comparative Trial of Aredia Versus Placebo for Prevention of Skeletal-Related Complications in Patients With Breast Cancer and Lytic Bone Lesions Treated With Chemotherapy. Phase II Open-Label, Multicenter Study of Single Agent Doxil in the Treatment of Patients With Anthracycline Resistant Locally Advanced or Metastatic Cancer. Assessment of the Predictive Value of the Extreme Drug Resistance (EDR) Assay in Patients Receiving Paclitaxel for Metastatic Breast Cancer. A Randomized, Double-Blind Trial Comparing Arimidex Alone With Nolvadex Alone With Arimidex and Nolvadex in Combination, as Adjuvant Treatment in Post-Menopausal Women With Breast Cancer. Comparison of the Effect of SCH 57050 and Anastrazole in Subjects With Breast Cancer Relapsing After an Initial Response to Tamoxifen or Showing Progression After Tamoxifen Given as Adjuvant to Surgery: A Prospective Double-Blind Phase III Trial. Daunoxome as First Line Therapy for the Treatment of Metastatic Breast Cancer. A Phase I/II Antibody MDX-H210 Combined With G-CSF in Patients With Metastatic Cancer That Over expresses HER2/neu. Adriamycin and Cytoxan Followed by Taxol or Taxotere either Weekly or Every Three Weeks for Women with Stage IIA, IIB or IIIA Breast Cancer with Six Lymph Nodes Removed. Medroxyprogesterone Acetate + Tamoxifen vs Observation + Tamoxifen in Post-Menopausal Women with Breast Cancer T1-3 N0-1 M0 Study of Tamoxifen and Raloxifene (STAR) for Prevention of Breast Cancer. Open-Label Study of Femara (2.5 mg) Daily for Patients with ER Receptor Positive Advanced Breast Cancer A Phase 2, Open-label., Randomized Clinical Trial of Skin Toxicity Treatment of Subjects Receiving Second-line FOLFIRI or Irinotecan Only Chemotherapy Concomitantly with Panitumumab. A multicenter, randomized double-blind placebo controlled phase III study of the efficacy of Xaliproden in preventing Randomized, open-label phase IIIB trial comparing two methods of Avastin-based induction/maintenance therapy for the first line treatment of MCRC A randomized, open-label, controlled, clinical trial of chemotherapy and Bevacizumab with/without XXXXX in the first line treatment of patients with mCRC A randomized, double-blind, placebo-controlled, phase III study in patients with mCRC or rectum who are receiving first-line chemotherapy with oxaliplatin/5-FU/leukovorine and PTK787/zk xxxxx or placebo An Open Label Randomized Phase III Study of Intermittent Oral Capecitabine in Combination with Intravenous Oxaliplatin (Q3W) (“XELOX”) versus Bolus and Continuous Infusion Fluorouracil/Intravenous Leukovorin with Intravenous Oxaliplatin (Q2W) (“FOLFOX4”) as First Line Treatment for Patients with Locally Advanced or Metastatic Colorectal Cancer. A Phase III Randomized, Open-Label, Multicenter Study of Irinotecan and Cetuximab vs. Irinotecan as a Second Line Treatment in Patients with Metastatic EGFR-Positive Colorectal Cancer. Phase III Intergroup Study, Postoperative Evaluation of 5-FU By Prolonged Venous Infusion Prior To And Following Combined Prolonged Venous Infusion Plus Pelvic XTR Versus Bolus 5-FU Plus Leucovorin Plus Levamisole Prior To And Following Combined Pelvic XRT In Patients With Rectal Cancer A Phase III, Multicenter, Randomized, Active-Controlled Clinical Trial to Evaluate the Efficacy and Safety of rhuMAb VEGF (Bevacizumab) in Combination with Standard Chemotherapy in Subjects with mCRC; Second-line Treatment of rhuMAb VEGF with or without Chemotherapy for Subjects whose Cancer Progressed on the Protocol An Open-Label, Single-Arm Trial of Patients with Metastatic Colorectal Cancer Receiving Irinotecan, 5-Fluorouracil, and Leucovorin Followed by Leukine® (Sargramostim), a Recombinant Human Granulocyte Macrophage Colony Stimulating Factor (GM-CSF) Hoffmann-La Roche MO16461: An Open-Label Phase II Study of Intermittent Oral Capecitabine in Combination with Intravenous Irinotecan (Q3W) in Patients with Advanced and/or Metastatic Colorectal Cancer A Phase II Trial of Trimetrexate, 5-Flurouracil and Leucovorin in Previously Treated Patients With Unresectable or Metastatic Colorectal Cancer. A Multicenter, Randomized Phase II Trial of Gemcitabine Plus 5FU/Leucovorin (FFG) vs. Oxaliplatin Plus 5FU/Leucovorin (FOLFOX4) as therapy for Patients with Metastatic Colorectal Cancer Therapeutic and Biological Effects of the Bispecific Antibody MDX-H210 Combined With GM-CSF in Patients With HER2/neu Positive Advanced Colorectal Carcinoma. A Randomized Multicenter Phase III Trial of Irinotecan in Combination with Three Different Methods in Administration of Fluoropyrimidine: Infusional 5-FU (FOLFIRI), Bolus 5-FU (Day 1 & 8), and Oral Capecitabine (Day 1-14); with Celecoxib versus Placebo as First Line Treatment for Patients with Metastatic Colorectal Cancer A Prospective, Randomized, Multi center Phase III Clinical Trial Comparing the Effects of PANOREX (17-1A Monoclonal Antibody) Injection Plus 5-Fluorouracil-Based-Chemotherapy Versus 5-Fluorouracil-Based-Chemtherapy Alone in Patients With Surgically Resected Stage III Carcinoma of the Colon. A Phase II, Randomized, Multicenter Comparison of the Efficacy of Oxaliplatin in Four Schedules of 5-FU with and without Leucovorin in Previously Untreated Advanced Colorectal Cancer A Phase II Study of Orzel Given as a Twice Daily Regimen in the Treatment of Patients with Metastatic Colorectal Cancer An Open-Label, Single-Arm Trial of Patients with Metastatic Colorectal Cancer Receiving Irinotecan, 5-Fluorouracil, and Leucovorin Followed by Leukine, a Recombinant Human Granulocyte-Macrophage Colony Stimulating Factor (GM-CSF) A Treatment Access Program with Oxaliplatin for Previously Treated Colorectal Cancer. An Open-Label Randomized Phase III Study Comparing Xeloda with IV Bolus 5-FU Combination with Low Dose Leucovorin as Adjuvant Chemotherapy Patients who Underwent Surgery for Dukes C Colon Cancer. CERVICAL CANCER Radiation plus Cisplatin versus Radiation plus 5-FU Infusion Protracted in the Treatment of Stage IIB, IIIB, and IVA Cervical Cancer. ENDOMETRIAL CANCER Cisplatin plus Doxorubicin or Cisplatin plus Doxorubicin plus Taxol with GCSF Support in the Treatment of Stage III-IV Primary or Recurrent Endometrial Cancer. Estrogen Replacement Therapy versus Placebo in the Treatment of Stage I-II Endometrial Adenocarcinoma. HEAD AND NECK CANCER Phase III of Radiation Therapy + or - Amifostine in Patients With Head and Neck Cancer. GASTRIC CANCER Open Label, Randomized Multicenter Phase II/III Study of Docetaxel in Combination with Cisplatin (CDDP) or Docetaxel in Combination with 5-FU and CDDP Compared to the Combination of CDDP and 5-FU in Patients with Metastatic or Locally Recurrent Gastric Cancer Previously Untreated with Chemotherapy for Advanced Disease. A Double-Blind, Randomized, Placebo-Controlled Study of the Efficacy and Safety of Epoetin Alfa Administered Weekly in Patients with Gastric or Rectal Cancers Undergoing Preoperative Chemo radiation Followed by Surgery HEMATOLOGIC MALIGNANCIES A Prospectively Randomized, Phase III, Multicenter, Controlled Trial to Evaluate the Safety and Efficacy of the Zevalin Therapeutic Regimen Plus Rituxan Compared with Rituxan Alone in Patients with Relapsed or Refractory Follicular Non-Hodgkin’s Lymphoma Treatment of Intermediate / High Grade NHL with Rituxan Combined With ESHAP Chemotherapy
Daunoxome and Dexamethasone Therapy With GM-CSF Support for Patients With Multiple Myeloma: A Phase II International Oncology Study Group (ISOG) Protocol. A Multi center, Open-Label Study Evaluating the Efficacy and Safety of Rituxan (Rituximab) in Combination with Six Cycles of Cyclophosphamide, Doxorubicin, Vincristine, Prednisone (CHOP) Followed by Rituxan Maintenance as Initial Therapy for Patients with Advanced Stage Indolent Non-Hodgkin’s Lymphoma HIGH DOSE THERAPY Phase II Study of High Dose Melphalan With Hematopoietic Stem Cell Support and GM-CSF in Refractory Multiple Myeloma. Sequential High-Dose Cyclophosphamide and High Dose BCNU/Etoposide/Melphalan Followed by Hematopoietic Rescue in Patients With Multiple Myeloma. High Dose Chemotherapy and Hematopoietic Stem Cell Rescue as Consolidation Therapy During First Complete or Partial Remission in Patients With Poor Risk Aggressive Lymphoma. High Dose Etoposide, Cyclophosphamide and Either Fractionated Total Body Irradiation or Carmustine With Autologous Bone Marrow Rescue for Refractory or Relapsed Hodgkin’s Disease. Sequential High Dose Cyclophosphamide and High Dose BCNU/Etoposide/Melphalan Followed by Hematopoietic Rescue in Patients With Lymphoma in “Sensitive” Relapse. LUNG CANCER “DARTMOUTH STUDY” A Multicenter, Randomized Phase III Study of Taxotere and Carboplatin VERSUS Taxotere and Gemcitabine in Patients with Advanced Non Small Lung Cancer. Randomized phase III trial comparing Targretin capsules/Carboplatin/Paclitaxel vs. Carboplatin/Paclitaxel in chemotherapy-naïve patients with Advanced (IIIB with Pleural Effusion) or Metastatic Non Small Cell Lung Cancer 104864/535 A Phase II Trial of Twice Daily Oral Topotecan as a Radiation Sensitizer with Twice Daily Radiotherapy for Newly Diagnosed Small Cell Lung Cancer Phase 3 Trial of Gemcitabine Plus Cisplatin Versus Cisplatin Alone in Patients With Locally Advanced or Metastatic Non-Small Cell Lung Cancer A Randomized Phase III Trial Surgery Alone or Surgery Plus Preoperative Paclitaxel / Carboplatin in Clinical Stage IB (T2N0), II (T1-2N1, T3N0) and Selected IIIA (t3N1) Non-Small Cell Lung Cancer (NSCLC) An Open-Label, Multicenter, Non-Comparative Study of Topotecan as Single Agent. Second-Line Therapy (Administered Intravenously as Five Daily Doses Every 21 Days) in Patients With Small Cell Cancer. Evaluation of Docetaxel and Cisplatin With Filgrastim Support for the Treatment of Patients With Stage III or IV Non-small Cell Lung Cancer. A Multi-Center Randomized Phase II Trial of Weekly Docetaxel plus Gemcitabine versus Weekly Paclitaxel plus Gemcitabine in Patients with Advanced or Metastatic Non-Small Cell Lung Cancer. A Phase IV, Open-Label, Prospective, Randomized, Multicenter Trial Comparing Quality of Life in Elderly Subjects receiving either Navelbine Injection, as a Single Agent or Best Supportive Care for the Treatment of Previously Untreated, Stage IV Non-Small Cell Lung Cancer. H3E-MC-JMEI: A Phase III Trial of Alimta versus Docetaxel in Patients Previously Treated with One Chemotherapy Regimen for Locally Advanced or Metastatic Non-Small Cell Lung Cancer A Phase III, Randomized, Double-Blind, Multi-Center Study of the Efficacy of Taxotere in Combination with Aptosyn versus Taxotere and Placebo in NSCLC Patients after Failure of Prior Platinum-Based Chemotherapy An Open-Label, Multicenter, Randomized Phase III Study of Hycamtin (Topotecan) as Single Agent, Second-Line Therapy (Administered Intravenously as Five Daily Doses Every 21 Days) Versus Second CAV In Patients With SCLC Who Have Relapsed at Least Three Months After Completion Of First-Line Therapy. A Randomized, Phase III Trial Comparing CPT-11 (Irinotecan HCL; Camptosar Injection)/ Cisplatin with Etoposide / Cisplatin in Patients with Previously Untreated, Extensive, Small-Cell Lung Cancer An Expanded Access Clinical Program with ZD1839 (Iressa™) for Patients with Advanced Non-small Cell Lung Cancer (NSCLC) The SILVA Study: Survival in an International Phase III Prospective Randomized LD Small Cell Lung Cancer Vaccination Study with Adjuvant BEC2 AND BCG. SWOG9909: Positron Emission Tomography (PET) Imaging of Lung Cancer Response to Therapy in Patients Registered to 9900 Open-Label Multicenter, Randomized Phase III Study of Topotecan as Single Agent, Second-Line Therapy (Administered Intravenously as Five Daily Doses Every 21 Days) Versus Taxol (Administered as a Three-Hour Infusion Every 21 Days) in Women With Advanced Epithelial Ovarian Carcinoma. Topotecan plus Cisplatin Induction Therapy Followed by Taxol PANCREATIC CANCER Modulation of 5-Fluorouracil With Trimetrexate and Leucovorin in Advanced Pancreatic Cancer. Phase III Randomized Study of RFS 2000 Versus Gemcitabine HCI in Chemonaive Pancreatic Cancer Patients Phase III Randomized Study of RFS 2000 Versus 5-FU in Pancreatic Cancer Patients that have Progressive Disease Following Gemcitabine HCI Treatment Janssen R115777-INT-16: A Randomized Phase II Trial to Evaluate the Efficacy of Gemcitabine plus R1157777 versus Gemcitabine plus Placebo on Time to Deterioration in Patients with Advanced Pancreatic Cancer. A Phase III Trial of Alimta Plus Gemzar versus Gemzar in Patients with Unresectable or Metastic Cancer of the Pancreas PROSTATE CANCER "A Phase III Randomized, Open-Label Study of CG1940 and CG8711 Versus Docetaxel and Prednisone in Patients with Metastatic Hormone-Refractory Prostate Cancer who are Chemotherapy Naïve Phase III randomized, open-label study of CG1940 and CG8711 vs. docetaxel & estrumustine in patients with metastatic hormone-refractory prostate cancer who are chemotherapy naïve A multicenter evaluation of combination chemotherapy and hormonal therapy using Taxol, Carboplatin, Estramustine and Lupron followed by definitive therapy for high-risk, locally advanced Prostate Cancer A Phase II Study to Determine the Biological Effects of Biospecific Antibody MDX-H210 (520C9XH22) Combined With GM-CSF in Patients With Advanced Prostate Cancer or Renal Cell Carcinomas That Express HER2/neu. A Phase II Trial of Epirubicin and Docetaxel in Patients with Hormone Refractory Prostate Cancer. SWOG9346: A Phase III Trial of Intermittent Androgen Deprivation in Patients with Stage D2 Prostate Cancer. SWOG9246: A Phase II Trial of Flutamide Withdrawal After Patients with Metastatic Prostate Cancer Have Had Disease Progression SUPPORTIVE THERAPY Double-Blind, Placebo-Controlled, Dose-Finding Study of the Effect of GTx-024 on Muscle Wasting (cachexia) in Patients with Cancer. A Pivotal Phase III, Observer-Blind, Randomized Clinical Trial of the Efficacy and Safety of APF530 Compared to Aloxi™ for the Prevention of Acute-onset and Delayed-Onset Chemotherapy-Induced Nausea and Vomiting Following the Administration of Either Moderately or Highly Emetogenic Chemotherapy Regimens. Surpass Study An Open Label Study to Assess Symptom Burden in Subjects with nonmyeloid Malignancies Receiving Chemotherapy and AranespTM PR00-03-006 A Double Blind, Randomized, Placebo-Controlled Study of The Efficacy and Safety of Epoetin Alfa Administered Weekly in Patients with Gastric or Rectal Cancers Undergoing Preoperative Chemoradiation Followed by Surgery. PR02-27-015 An Open-Labeled Pilot Study To Evaluate The Effects of High Dose PROCRIT® (Epoetin alfa) In Maintaining Hemoglobin Levels in Anemix Cancer Patients Receiving Chemotherapy On a Weekly or Every 4 Week Regimen. PR0-02-016 An Open Labeled Pilot Study To Evaluate The Effects Of High Dose PROCRIT® (Epoetin alfa) In Maintaining Hemoglobin Levels inAnemic Cancer Patients Receiving Chemotherapy on a Every 3 Week Regimen. PR00-27-012/225-05-00 Phase II: An Open Label Study of PROCRIT® (Epoetin Alfa) in Women Undergoing Adjuvant Chemotherapy for Stage I,II or III Breast Cancer A Double Blind, Multicenter, Crossover Study Comparing the Efficacy and Safety of Intravenous (IV) Granisetron Hydrochloride 10ug/kg With IV Ondansetron Hydrochloride 32 mg in the Prevention of Nausea and Vomiting Induced by IV Cyclophosphamide and Doxorubicin Chemotherapy in Patients With Breast Cancer. PALO-99-04: A Randomized, Double-Blind Comparison of Single-Dose Ondansetron Intravenous Versus Single-Dose Intravenous Granisetron on the Prevention of Nausea And Vomiting With High-Dose Cisplatin Chemotherapy. A Randomized, Double-Blind Comparison of Oral Ondansetron and Compazine for the Prevention of Nausea and Vomiting Associated With Moderately-Emetogenic Chemotherapy. A Pilot Study to Evaluate the Response Rate of Procrit at 40,000 Units Once Weekly in Anemic Cancer Patients Not Receiving Chemotherapy A Randomized, Double-Blind, Placebo-Controlled Study Conducted Under In-House Blinding Conditions to Determine the Efficacy and Tolerability of MK-0869 for the Prevention of Chemotherapy-Induced Nausea and Vomiting Associated with Moderately Emetogenic Chemotherapy An Open-Label, Uncontrolled, Multicenter Study to Evaluate the Efficacy and Safety of Two 1mg Tablets of Kytril (Granisetron Hydrochloride) Given Once Prior to Chemotherapy in the Prevention of Nausea and Vomiting Induced by Cisplatin-Based Chemotherapy. A Double Blind, Parallel, Multicenter Study Comparing the Efficacy And Safety of Intravenous Granisetron and Ondansetron in the Prophylaxis of Nausea and Emesis Induced by Cisplatin-Based Chemotherapy. A Phase III Randomized, Double Blind, Placebo-Controlled Study to Evaluate the Effects of Fragmin in Preventing CRCs when Given Daily to Cancer Patients with Central Venous Catheters A Double-Blind, Multicenter, Parallel Study, Comparing the Efficacy and Safety of Oral Granisetron Hydrochloride 2 mg With IV Ondansetron Hydrochloride 32mg, Given Once, in the Prevention of Nausea and Vomiting Induced by IV Cyclophosphamide-Based or Carboplatin-Based Chemotherapy In Patients With Malignant Disease. A Randomized, Double-Blind, Placebo-Controlled Comparison of the Analgesic Activity of Valdecoxib 40 mg BID as Add On Therapy to Opioid Medication in Patients with Chronic Cancer Pain. A Randomized Dose-Finding Study of NESP Administered by SQ Injection for the Treatment of Anemia in Subjects with Solid Tumors Receiving Multicycle Chemotherapy A Phase IV Open Label Study of Procrit in Women Receiving Adjuvant Chemotherapy for Breast Cancer A Double Blind, Efficacy and Safety Study of the Oral Direct Thrombin Inhibitor, H376/95 versus Standard Therapy in Patients with Active, Symptomatic DVT with or without PE. A Dose-Finding Study of NESP Administered by SQ Injection for the Treatment of Anemia of Subjects with Chronic Anemia of Cancer. A Randomized, Open-Label, Multicenter Study of Subcutaneous and Intravenous Administration of Darbepoetin Alfa (Novel Erythropoiesis Stimulating Protein, NESP) for the Treatment of Anemia in Subjects with Non-Myeloid Malignancies Receiving Multicycle Chemotherapy A Randomized Open-Label Study of Darbepoetin Alfa (Novel Erythropoiesis Stimulating Protein, NESP) and rHuEPO for the Treatment of Anemia in Subjects with Non-Myeloid Malignancies Receiving Multi-Cycle Chemotherapy A Phase III, International, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study of Innopep (Tinzaparin Sodium) for Primary Prevention of Venous Thromboembolism and Reduction of Mortality in Subjects with Advanced Cancer Interleukin Eleven (Neumega rhIL-11 Growth Factor at a Dose of 50ug/kg Randomized, Double-Blind, Acyclovir-Controlled, Multicenter Study to Assess the Safety, Efficacy and Pharmacokinetics of Intravenous Penciclovir for the Treatment of Mucocutaneous Herpes Simplex Infection in Immuno-compromised Patients. EDUCATION 6/73 - 6/78 University of Bombay, India 6/70 - 10/72 University of Bombay, India 9/03 – 8/05 University of California, Irvine – Paul Merage School of Business RESIDENCY 7/83 - 6/84 Kaiser Permanente, West Los Angeles, California 7/82 - 6/83 Martin Luther King, Jr./Drew Medical Center, Los Angeles, California 7/81 - 6/82 St. Joseph Mercy Hospital, Michigan 8/80 - 6/81 St. Joseph Mercy Hospital, Michigan 8/79 - 5/80 Nair Hospital, India 7/78 - 7/79 Nair Hospital, India 7/87 - 6/88 University of Southern California, West Los Angeles, California 7/85 - 6/87 Kaiser Permanente, (Sunset) Los Angeles, California 7/84 – 6/85 Kaiser Permanente, West Los Angeles, California PUBLICATIONS · Evaluation of Docetaxel and Cisplatin With Filgrastim Support for the treatment of Patients With Stage III or IV Non-small Cell Lung Cancer H.Jhangiani, G.R.Justice, et al - American Society of Clinical Oncology, San Francisco, California, May 2001 Ring-Shaped Particle (RSP): A Tumor Marker for Lung and Ovarian Cancer Correlates Well as a Parameter of Tumor Response to Therapy: R. Guerrero, G. Justice, D. Rounds, K. Shah, H. Jhangiani, N. Tchekmedyan, P. Coluzzi, F. Dexeus, T. White, E. Bald-American Society of Clinical Oncology, Orlando, Florida, April 1993 Ring-Shaped Particle (RSP): A New Tumor Marker Published, USA for Breast, Lung Cancer That Accurately Discriminated between Primary Lung Cancer and Normal s, Including Chronic Obstructive Pulmonary Disease (COPD) and Smokers: Presented to American Society of Clinical Oncology, San Diego, CA May 1992. Finding an effective dose of fentanyl effervescent buccal tablets: Combined results of open-label titration: M.S. Wertheim, H. Jhangiani, G. Niebler, V. Charu – Journal of Clinical Oncology, 2006 ASCO Annual Meeting Proceedings Part I. Vol. 24, No. 18S (June Supplement), 2006.
BOARD CERTIFICATION Medical Oncology, November 1989 LICENSURE California License # A38872; DEA# AJ1756937 / DEA# BJ 7758658 RESEARCH AFFILIATIONS Member of Southwest Oncology Group (SWOG) REGIONAL AFFILIATION Regional Medicare Representative for the State of California for Medical Oncology Association of Southern California – California Oncology Consortium SPEAKING AFFILIATIONS Amgen Speakers Bureau - Aranesp PRECEPTOR USC/Norris Cancer Center - USC/LA County Medical Center LIAISON POSITIONS MEDICAL EXAMINER Orange County Employees Retirement System, Santa Ana, Orange County, California
MEMBERSHIPS Orange Country Medical Association AWARDS Orange County Medical Association Physician of Excellence Award 2006 BIOGRAPHICAL Date of Birth: March 14, 1954 |
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