Dr. Gupta graduated from the Gov't Med Coll, Baba Farid Univ Hlth Sci, Patiala, Punjab, India in 1973. He works in Clifton, NJ and 1 other location and specializes in Gastroenterology and Internal Medicine. Dr. Gupta is affiliated with Chilton Medical Center, Saint Marys General Hospital, St Josephs Regional Medical Center and St Josephs Wayne Hospital.
Dr. Gupta graduated from the Gov't Med Coll, Guru Nanak Dev Univ, Amritsar, Punjab, India in 1975. He works in Lansing, MI and 2 other locations and specializes in Internal Medicine and Sleep Medicine. Dr. Gupta is affiliated with Eaton Rapids Medical Center, Mclaren Orthopedic Hospital and Sparrow Hospital.
Henry Ford Medical GroupAshok K Gupta MD 2111 Orch Lk Rd, Keego Harbor, MI 48320 2486816577 (phone), 2487327136 (fax)
Education:
Medical School Gov't Med Coll, Baba Farid Univ Hlth Sci, Patiala, Punjab, India Graduated: 1972
Languages:
English Spanish
Description:
Dr. Gupta graduated from the Gov't Med Coll, Baba Farid Univ Hlth Sci, Patiala, Punjab, India in 1972. He works in Sylvan Lake, MI and specializes in Internal Medicine and Internal Medicine - Geriatrics. Dr. Gupta is affiliated with Doctors Hospital Of Michigan.
Medical School University of Nebraska College of Medicine Graduated: 1996
Languages:
English
Description:
Dr. Gupta graduated from the University of Nebraska College of Medicine in 1996. He works in Las Vegas, NV and 2 other locations and specializes in Diagnostic Radiology. Dr. Gupta is affiliated with Desert Springs Hospital Medical Center, Spring Valley Hospital Medical Center, Summerlin Hospital Medical Center, University Medical Center Of Southern Nevada and Valley Hospital Medical Center.
Henry Ford Medical GroupHenry Ford Medical Center Fairlane 19401 Hubbard Dr, Dearborn, MI 48126 3139828100 (phone), 3139828205 (fax)
Education:
Medical School M.g.m. Med Coll, Devi Ahilya Vishwavidhyalaya, Indore, Mp, India Graduated: 1975
Languages:
English Spanish
Description:
Dr. Gupta graduated from the M.g.m. Med Coll, Devi Ahilya Vishwavidhyalaya, Indore, Mp, India in 1975. He works in Dearborn, MI and specializes in Internal Medicine. Dr. Gupta is affiliated with Henry Ford Hospital, Henry Ford Macomb Hospital, Henry Ford West Bloomfield Hospital and Henry Ford Wyandotte Hospital.
Madison Cardiology 610 E 12 Mile Rd, Madison Heights, MI 48071 2485419111 (phone), 2485419113 (fax)
Education:
Medical School Gov't Med Coll, Guru Nanak Dev Univ, Amritsar, Punjab, India Graduated: 1974
Languages:
English
Description:
Dr. Gupta graduated from the Gov't Med Coll, Guru Nanak Dev Univ, Amritsar, Punjab, India in 1974. He works in Madison Heights, MI and specializes in Cardiovascular Disease and Internal Medicine. Dr. Gupta is affiliated with Saint John Macomb-Oakland Hospital and William Beaumont Hospital.
Wikipedia References
Ashok Kumar Gupta
Name / Title
Company / Classification
Phones & Addresses
Ashok Gupta Owner
Global Project Solutions Business Services
20223 Brondesbury Dr, Katy, TX 77450
Ashok Gupta Director, Manager
MARLIN STRATEGICS, LLC
3880 Greenhouse Rd STE 219, Houston, TX 77084 4400 Post Oak Pkwy, Houston, TX 77027 20223 Brondesbury, Katy, TX 77450
Ashok Gupta Chief Executive Officer
Aniotek, Inc Electronic Product Development and Consulting
10 April Dr, South Brunswick, NJ 08810 7322742648
Ashok Gupta
9-GLOBAL INSTITUTE OF MANAGEMENT AND LEADERSHIP, OHIO, INC
Ashok Gupta
GLOBAL INTERNATIONAL, LLC
Ashok Gupta
THE UNIVERSITY OF EAST CLEVELAND, INC
Ashok Gupta
9GLOBAL INSTITUTE OF APPLIED TECHNOLOGY, INC
Ashok Gupta
GETAX OCEAN TRADES PTE. LTD
Resumes
Chief, Receiving & Inspection Officer At United Nations Peace Keeping Mission
Senior Vice President - Energy Project Finance and Advisory Services at Mizuho Corporate Bank
Location:
Houston, Texas Area
Industry:
Banking
Work:
Mizuho Corporate Bank - Houston, Texas since 2005
Senior Vice President - Energy Project Finance and Advisory Services
CUNA Mutual Group - Houston, Texas 2004 - 2005
Financial Solutions Officer
BearingPoint - Erbil, Iraq 2003 - 2004
Senior Consultant
Global Project Associates - Houston 2002 - 2003
Principal
El Paso Corporation - Houston, Texas 2000 - 2002
Vice President - International Finance
Education:
The University of Texas at Austin
Master of Business Administration (MBA), Information Systems Management, Finance
University of St. Thomas (TX)
MSA, Accounting
Jadavpur University
Bachelor of Engineering (BE), Civil Engineering
Stacie M. Goldberg - Princeton NJ, US Ashok K. Gupta - Plainsboro NJ, US Xi Tao Wang - Wellesley MA, US John M. Wigginton - Collegeville PA, US
International Classification:
C07K 16/28
US Classification:
4241721, 5303882
Abstract:
The disclosure provides a method for immunotherapy of a subject afflicted with cancer, comprises administering to the subject a composition comprising a therapeutically effective amount of an antibody that inhibits signaling from the PD-1/PD-L1 signaling pathway. This disclosure also provides a method for immunotherapy of a subject afflicted with cancer comprising selecting a subject that is a suitable candidate for immunotherapy based on an assessment that the proportion of cells in a test tissue sample from the subject that express PD-L1 on the cell surface exceeds a predetermined threshold level, and administering a therapeutically effective amount of an anti-PD-1 antibody to the selected subject. The invention additionally provides rabbit mAbs that bind specifically to a cell surface-expressed PD-L1 antigen in a FFPE tissue sample, and an automated IHC method for assessing cell surface expression in FFPE tissues using the provided anti-PD-L1 Abs.
- GAITHERSBURG MD, US JOHN ANDREW BLAKE-HASKINS - GAITHERSBURG MD, US MAGDALENA ZAJAC - CAMBRIDGE, GB MARLON REBELATTO - GAITHERSBURG MD, US ASHOK GUPTA - GAITHERSBURG MD, US TONY HO - GAITHERSBURG MD, US JILL WALKER - CAMBRIDGE, GB XIAOPING JIN - GAITHERSBURG MD, US SHANNON MORRIS - GAITHERSBURG MD, US ROBERT IANNONE - GAITHERSBURG MD, US LI SHI - GAITHERSBURG MD, US MOHAMMED DAR - GAITHERSBURG MD, US YONG BEN - GAITHERSBURG MD, US
International Classification:
C07K 16/28 A61P 35/00 A61K 9/00 G01N 33/542
Abstract:
Provided are methods of treating bladder cancer (e.g., urothelial carcinoma, UC) in a subject having bladder cancer, e.g., UC, with an effective dose regimen of an anti-PD-L1 antibody, e.g., durvalumab, or an antigen binding fragment thereof. Also provided are methods in which an anti-PD-L1 antibody is used in combination with another immunotherapeutic agent, e.g., tremelimumab to treat a bladder cancer, e.g., UC, in a subject having bladder cancer. In some cases, the subject undergoing treatment is identified as having a bladder cancer or tumor that is PD-L1-low/neg, or PD-L1-high. Methods are also provided in which anti-PD-L1 antibody treatment of bladder cancer is used following a standard of care or first-line therapy in subjects who have progressed following such therapies or who have relapsed after a prior treatment regimen.
Cancer Immunotherapy By Disrupting Pd-1/Pd-L1 Signaling
- Princeton NJ, US Stacie M. Goldberg - Potomac MD, US Ashok K. Gupta - Clarksburg MD, US Xi-Tao Wang - Wellesley MA, US Jon M. Wigginton - Collegeville PA, US
Assignee:
Bristol-Myers Squibb Company - Princeton NJ
International Classification:
C07K 16/28 A61K 39/395 C07K 16/18 G01N 33/574
Abstract:
The disclosure provides a method for immunotherapy of a subject afflicted with cancer, comprises administering to the subject a composition comprising a therapeutically effective amount of an antibody that inhibits signaling from the PD-1/PD-L1 signaling pathway. This disclosure also provides a method for immunotherapy of a subject afflicted with cancer comprising selecting a subject that is a suitable candidate for immunotherapy based on an assessment that the proportion of cells in a test tissue sample from the subject that express PD-L1 on the cell surface exceeds a predetermined threshold level, and administering a therapeutically effective amount of an anti-PD-1 antibody to the selected subject. The invention additionally provides rabbit mAbs that bind specifically to a cell surface-expressed PD-L1 antigen in a FFPE tissue sample, and an automated IHC method for assessing cell surface expression in FFPE tissues using the provided anti-PD-L1 Abs.
- GAITHERSBURG MD, US JOHN ANDREW BLAKE-HASKINS - GAITHERSBURG MD, US MAGDALENA ZAJAC - CAMBRIDGE, GB MARLON REBELATTO - GAITHERSBURG MD, US ASHOK GUPTA - GAITHERSBURG MD, US TONY HO - GAITHERSBURG MD, US JILL WALKER - CAMBRIDGE, GB XIAOPING JIN - GAITHERSBURG MD, US SHANNON MORRIS - GAITHERSBURG MD, US ROBERT IANNONE - GAITHERSBURG MD, US LI SHI - GAITHERSBURG MD, US MOHAMMED DAR - GAITHERSBURG MD, US YONG BEN - GAITHERSBURG MD, US
International Classification:
C07K 16/28 A61K 9/00 G01N 33/542 A61P 35/00
Abstract:
Provided are methods of treating bladder cancer (e.g., urothelial carcinoma, UC) in a subject having bladder cancer, e.g., UC, with an effective dose regimen of an anti-PD-L1 antibody, e.g., durvalumab, or an antigen binding fragment thereof. Also provided are methods in which an anti-PD-L1 antibody is used in combination with another immunotherapeutic agent, e.g., tremelimumab to treat a bladder cancer, e.g., UC, in a subject having bladder cancer. In some cases, the subject undergoing treatment is identified as having a bladder cancer or tumor that is PD-L1-low/neg, or PD-L1-high. Methods are also provided in which anti-PD-L1 antibody treatment of bladder cancer is used following a standard of care or first-line therapy in subjects who have progressed following such therapies or who have relapsed after a prior treatment regimen.
Cancer Immunotherapy By Disrupting Pd-1/Pd-L1 Signaling
- Princeton NJ, US Stacie M. Goldberg - Potomac MD, US Ashok K. Gupta - Clarksburg MD, US Xi-Tao Wang - Wellesley MA, US Jon M. Wigginton - Collegeville PA, US
Assignee:
Bristol-Myers Squibb Company - Princeton NJ
International Classification:
C07K 16/28 A61K 39/395 C07K 16/18 G01N 33/574
Abstract:
The disclosure provides a method for immunotherapy of a subject afflicted with cancer, comprises administering to the subject a composition comprising a therapeutically effective amount of an antibody that inhibits signaling from the PD-1/PD-L1 signaling pathway. This disclosure also provides a method for immunotherapy of a subject afflicted with cancer comprising selecting a subject that is a suitable candidate for immunotherapy based on an assessment that the proportion of cells in a test tissue sample from the subject that express PD-L1 on the cell surface exceeds a predetermined threshold level, and administering a therapeutically effective amount of an anti-PD-1 antibody to the selected subject. The invention additionally provides rabbit mAbs that bind specifically to a cell surface-expressed PD-L1 antigen in a FFPE tissue sample, and an automated IHC method for assessing cell surface expression in FFPE tissues using the provided anti-PD-L1 Abs.
Cancer Immunotherapy By Disrupting Pd-1/Pd-L1 Signaling
- Princeton NJ, US Stacie M. Goldberg - Potomac MD, US Ashok K. Gupta - Clarksburg MD, US Xi-Tao Wang - Wellesley MA, US Jon M. Wigginton - Collegeville PA, US
Assignee:
Bristol-Myers Squibb Company - Princeton NJ
International Classification:
C07K 16/28 A61K 39/395 C07K 16/18 G01N 33/574
Abstract:
The disclosure provides a method for immunotherapy of a subject afflicted with cancer, comprises administering to the subject a composition comprising a therapeutically effective amount of an antibody that inhibits signaling from the PD-1/PD-L1 signaling pathway. This disclosure also provides a method for immunotherapy of a subject afflicted with cancer comprising selecting a subject that is a suitable candidate for immunotherapy based on an assessment that the proportion of cells in a test tissue sample from the subject that express PD-L1 on the cell surface exceeds a predetermined threshold level, and administering a therapeutically effective amount of an anti-PD-1 antibody to the selected subject. The invention additionally provides rabbit mAbs that bind specifically to a cell surface-expressed PD-L1 antigen in a FFPE tissue sample, and an automated IHC method for assessing cell surface expression in FFPE tissues using the provided anti-PD-L1 Abs.
Cancer Immunotherapy By Disrupting Pd-1/Pd-L1 Signaling
- Princeton NJ, US Stacie M. Goldberg - Potomac MD, US Ashok K. Gupta - Clarksburg MD, US Xi-Tao Wang - Wellesley MA, US Jon M. Wigginton - Collegeville PA, US
Assignee:
Bristol-Myers Squibb Company - Princeton NJ
International Classification:
C07K 16/28 A61K 39/395 C07K 16/18 G01N 33/574
Abstract:
The disclosure provides a method for immunotherapy of a subject afflicted with cancer, comprises administering to the subject a composition comprising a therapeutically effective amount of an antibody that inhibits signaling from the PD-1/PD-L1 signaling pathway. This disclosure also provides a method for immunotherapy of a subject afflicted with cancer comprising selecting a subject that is a suitable candidate for immunotherapy based on an assessment that the proportion of cells in a test tissue sample from the subject that express PD-L1 on the cell surface exceeds a predetermined threshold level, and administering a therapeutically effective amount of an anti-PD-1 antibody to the selected subject. The invention additionally provides rabbit mAbs that bind specifically to a cell surface-expressed PD-L1 antigen in a FFPE tissue sample, and an automated IHC method for assessing cell surface expression in FFPE tissues using the provided anti-PD-L1 Abs.
Cancer Immunotherapy By Disrupting Pd-1/Pd-L1 Signaling
- Princeton NJ, US Stacie M. Goldberg - Potomac MD, US Ashok K. Gupta - Clarksburg MD, US Xi-Tao Wang - Wellesley MA, US Jon M. Wigginton - Collegeville PA, US
Assignee:
Bristol-Myers Squibb Company - Princeton NJ
International Classification:
C07K 16/28 G01N 33/574 C07K 16/18 A61K 39/395
Abstract:
The disclosure provides a method for immunotherapy of a subject afflicted with cancer, comprises administering to the subject a composition comprising a therapeutically effective amount of an antibody that inhibits signaling from the PD-1/PD-L1 signaling pathway. This disclosure also provides a method for immunotherapy of a subject afflicted with cancer comprising selecting a subject that is a suitable candidate for immunotherapy based on an assessment that the proportion of cells in a test tissue sample from the subject that express PD-L1 on the cell surface exceeds a predetermined threshold level, and administering a therapeutically effective amount of an anti-PD-1 antibody to the selected subject. The invention additionally provides rabbit mAbs that bind specifically to a cell surface-expressed PD-L1 antigen in a FFPE tissue sample, and an automated IHC method for assessing cell surface expression in FFPE tissues using the provided anti-PD-L1 Abs.