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Eric Whitman

Dr. Eric Whitman MD

Medical Director, Office of Grants and Research, ATLANTIC HEALTH SYSTEM INC

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Member of the Healthcare Council

Council Member Biography

Eric Whitman, MD, is the Medical Director of the Office of Grants and Research for Atlantic Health System in Morristown, New Jersey. He is a board certified General Surgeon with fellowship training in surgical oncology. He specializes in melanoma care, endocrine and oncologic surgery. Dr. Whitman is also the founding Director of the Atlantic Health Melanoma Center, a clinical and research Center of Excellence within the Carol G. Simon Cancer Center of Morristown Memorial Hospital and Overlook Hospital. He specializes in endocrine and oncologic surgery, with particular emphasis in melanoma care and minimally-invasive endocrine surgery for diseases of the thyroid, parathyroid, and adrenal glands. Dr. Whitman has an active surgical practice and participates in multiple research studies to treat melanoma, with particular interest in novel combinations of immunotherapeutic, chemotherapeutic, and targeted agents. (This is me - Update Profile)


Employment History

2007 - 2007
Medical Director of Cancer Center, Mountainside Hospital
2006 - Unspecified
Medical Director, Office of Grants and Research, ATLANTIC HEALTH SYSTEM INC
2004 - 2007
Chairman/Admin Director, Mountainside Hospital
2004 - Unspecified
Founding Director of Melanoma Center, ATLANTIC HEALTH SYSTEM
1998 - 2004
Partner, CIO, SUBURBAN SURGICAL ASSOCIATES
1992 - 1998
Assistant Professor, THE WASHINGTON UNIVERSITY

GLG NewsSM Analyses by Eric Whitman(?)

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Synta Drug for Metastatic Melanoma Not Dead Yet (?)

November 3, 2009

Synta Pharmaceuticals Announces Updated Elesclomol SYMMETRYSM Data Presented at Melanoma XIII | www.businesswire.com

Updated data presented at an annual Melanoma conference suggests the drug Elesclomol may benefit a subset of patients treated on a Phase III trial. This Synta Pharmaceuticals-sponsored trial in metastatic melanoma patients was stopped for safety (survival) concerns in February 2009, but the updated analysis suggests that a commonly available biomarker may identify patients who appear to benefit from Elesclomol treatment.This news is important because it may allow Synta to continue to pursue approval for Elesclomol in either melanoma patients or in other cancers. They will report an updated survival analysis twelve months after the protocol was stopped, after February 2010. Further info from Synta is expected soon.

Delcath Phase III trial for metastatic melanoma completes enrollment

November 3, 2009

Delcath Systems, Inc. Completes Phase III Study Enrollment | www.reuters.com

The Delcath Systems Percutaneous Hepatic Perfusion (PHP) trial to treat patients with metastatic melanoma has completed enrollment and now must track patients, record data, and analyze results.This trial was apparently enrolled on schedule and the company is targeting 2010 for FDA regulatory submission.

Plexxikon Drug for Melanoma Continues to Show Great Promise

October 14, 2009

Researchers herald 'breakthrough' skin cancer therapy | www.fiercebiotech.com

The new drug PLX-4032, being developed by Plexxikon and Roche, continues to show impressive short term results in melanoma patients with specific BRAF mutations, with a reported 70% tumor response rate.

Gleevec shows promise as targeted melanoma treatment

July 27, 2009

A phase II study of imatinib mesylate (IM) for patients with advanced melanoma harboring somatic alterations of KIT | meeting.ascopubs.org

Gleevec (Imatinib), a target specific cancer treatment drug against KIT oncogene mutations, shows early evidence of efficacy in treating melanomas with susceptible genetic mutations, further support for a personalized medicine, targeted therapy, approach to treating melanoma and cancers in general.

PLX-4032, the new great hope for targeted therapy in melanoma

July 27, 2009

Plexxikon announces PLX4032 Phase I Data showing objective responses in metastatic melanoma patients | www.plexxikon.com

PLX-4032, a Plexxikon drug being co-developed with Roche, has shown remarkable results in a Phase I trial for melanoma and appears poised for rapid progression through Phase II and Phase III testing with perhaps accelerated FDA approval on the horizon.

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