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Management
• Michael Fonstein,
Ph.D.
Chief Executive Officer and President
• Andrei Gudkov, Ph.D., D. Sci.
Chief Scientific Officer
• Yakov Kogan, Ph.D., MBA
Chief Operating Officer
• Jack Marhofer, MBA, CMA, CFM
Chief Financial Officer
• Farrel Fort, Ph.D., MBA, DABT
Senior Vice President, Drug Development
• Michael Kurman, MD
Chief Medical Officer
• Ed Venkat, Ph.D.
Director of Vice President, Pharmaceutical Development
• Donald Handley, MBA.
Director, Regulatory Affairs
• Michael Paterno, O.D.
Director, Clinical Operations

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Michael
Fonstein, Ph.D.
Chief Executive Officer and President
Dr. Fonstein has served as the company's Chief Executive Officer
and President since the company's inception in June 2003.
He served as Director of the DNA Sequencing Center at the
University of Chicago from its creation in 1994 to 1998, when
he left to found Integrated Genomics, Inc. located in Chicago,
Illinois. He served as CEO and President of Integrated Genomics
from 1997 to 2003. Dr. Fonstein has won several business awards,
including the Incubator of the Year Award from the Association
of University Related Research Parks. He was also the winner
of a coveted KPMG Illinois High Tech Award. |

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Andrei
Gudkov, Ph.D., D. Sci.
Chief Scientific Officer
Dr. Gudkov has served as one of the company's directors and
as the company's Chief Scientific Officer since the company's
inception in June 2003. Prior to 1990, he worked at The National
Cancer Research Center in Moscow (USSR) where he led a broad
research program focused on virology and cancer drug resistance.
In 1990, he reestablished his lab at the University of Illinois
at Chicago where he became a tenured faculty member in the
Department of Molecular Genetics. His lab concentrated on
the development of new functional gene discovery methodologies
and the identification of new candidate cancer treatment targets.
In 1999, he defined p53 as a major determinant of cancer treatment
side effects and suggested this protein as a target for therapeutic
suppression. In 2001, Dr. Gudkov moved his laboratory to the
Lerner Research Institute at the Cleveland Clinic where he
became Chairman of the Department of Molecular Biology and
Professor of Biochemistry at Case Western Reserve University.
In 2007, Dr. Gudkov accepted the position of Senior VP Basic
Science and Chair, Department of Cell Stress Biology at Roswell
Park Cancer Institute in Buffalo, NY. Dr. Gudkov is not employed
full time by the company, but rather divides time between
work for CBLI and for Roswell Park. |

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Yakov
Kogan, Ph.D., MBA
Chief Operating Officer
Dr. Kogan has served as one of the company's directors and
as the company's Executive Vice President of Business Development
since the company's inception in June 2003 and as Secretary
since March 2006. From 2001 to 2004, as Director for Business
Development at Integrated Genomics, he was responsible for
commercial sales and expansion of the company's capital base.
Prior to his tenure in business development, Dr. Kogan worked
as a Group Leader/Senior Scientist at Integrated Genomics
and ThermoGen, Inc. and as Research Associate at the University
of Chicago. Dr. Kogan holds a Ph.D. degree in Molecular Biology
from VNII Genetica, as well as an M.S. degree in Biology from
Moscow State University. |

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Jack
Marhofer, MBA, CMA, CFM
Chief Financial Officer
Mr. Marhofer joined us as the Controller and General Manager
in February 2005 and was subsequently appointed to be the
company's Chief Financial Officer in August 2005. He was Corporate
Controller of Litehouse Products, Inc. from June 2001 to February
2005. He obtained certifications as a Certified Managerial
Accountant and Certified Financial Manager in March 2006.
Mr. Marhofer earned his Bachelor of Science in Accounting
and Marketing from Miami University in Ohio in 1984, and his
Masters in Business Administration in Finance from Akron University
in Ohio in 1997, where he was named to the National Honor
Society of the Financial Management Association. |

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Michael
Kurman, MD
Chief Medical Officer
Dr. Kurman joined Cleveland BioLabs, Inc. as Chief Medical
Officer in January 2008. He has spent over twenty-five years
in the oncology drug development field. Dr. Kurman is a board
certified medical oncologist who practiced community oncology
in New Jersey, where he participated as an investigator in
oncology clinical trials sponsored by the Eastern Cooperative
Oncology Group (ECOG) and the Memorial Adjunct Staff Oncology
Group (MASOG). During his career in the pharmaceutical industry,
he has held positions of progressive responsibility at Janssen
Research Foundation as Director of Oncology, at Cyotgen Corporation
as Senior Director of Research and at U.S. Bioscience as Vice-President
for Research. Prior to establishing his consultancy, Dr. Kurman
served as Vice-President for Clinical and Scientific Operations
for Quintiles’ Oncology Therapeutics Division. In his nineteen-year
career in the pharmaceutical industry, Dr. Kurman has been
involved in the regulatory review or commercial launch of
four new oncology products. Dr. Kurman received his bachelor’s
degree summa cum laude in biology from Syracuse University
and his M.D. degree from Cornell University Medical College.
He received his training in internal medicine at the State
University of New York – Upstate Medical Center, and his oncology
training at Mt. Sinai Medical Center in New York. Dr. Kurman
serves on the scientific advisory boards of several companies
as well as serving on the board of Avalon Pharmaceuticals,
where he is head of the compensation committee, and of Thallion
Pharmaceuticals. Dr. Kurman is also an Adjunct Associate Professor
of Epidemiology and Health Promotion in the Master of Clinical
Trials Program at New York University and an Adjunct Professor
for Pharmaceutical Technology Management at the Wesley J.
Howe School of Technology Management of Stevens Institute
of Technology. |

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Ed
Venkat, Ph.D.
Vice President, Pharmaceutical Development
Ed Venkat, Ph.D. joined Cleveland BioLabs, Inc. as Director
of Chemistry, Manufacturing and Controls in 2006. He has over
twenty years of experience with demonstrated leadership capability
in drug development, operation and management of commercial
cGMP manufacturing, process engineering, technology transfer,
and regulatory and quality control systems. Dr. Venkat has
drug development and manufacturing experience with biological
compounds and small molecules in both Big Pharma and small
biotech. Before joining CBLI, he worked in numerous research
and managerial positions at Merck & Co, Inc. (Rahway,
NJ) and as the Director of Process Development for GlobeImmune,
Inc. (Louisville, CO). In addition to a B.S. degree in Chemical
Engineering, Dr. Venkat holds an M.S. degree in Biochemical
Engineering from The Indian Institute of Technology (New Delhi,
India), a Ph.D. in Chemical and Biochemical Engineering from
Rutgers University (New Brunswick, NJ) and a M.S. degree in
Executive Technology Management from Stevens Institute of
Technology in Hoboken, NJ.
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Donald Handley, MBA
Director, Regulatory Affairs
Mr. Handley joined Cleveland BioLabs in 2010. Prior to joining CBLI, Mr. Handley was Director of Global Regulatory Affairs at Bausch & Lomb, Inc., where he directed submissions of several New Drug Applications and Investigational New Drug Applications, led preparation efforts for a successful FDA advisory committee meeting and multiple other FDA interactions and was involved in meetings with international regulatory authorities. From 1999 to 2002, Handley held the positions of Manager and then Senior Manager of Regulatory Affairs at Celltech / Medeva Pharmaceuticals Inc. From 1996 to 1999, he served as Senior Regulatory Affairs Associate and then Manager of Worldwide Regulatory Affairs at Bristol-Myers Squibb Company. Before this, he held several positions in Regulatory Affairs at Fisons Pharmaceuticals. Handley holds a Bachelor of Science in Biochemical Pharmacology from the State University of New York at Buffalo, a Master of Science in Natural Sciences from the Roswell Park Cancer Institute Graduate Division of the State University of New York at Buffalo and a Master of Business Administration from the State University of New York at Buffalo.
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Michael Paterno, O.D.
Director, Clinical Operations
Dr. Paterno joined Cleveland BioLabs in 2010. He brings twenty years of clinical research and development experience to the company. Prior to joining CBLI, Paterno was Manager, Pharmaceutical Clinical Science at Bausch & Lomb, Inc., where he led teams in the design, implementation, and conduct of Phase I – IV clinical trials in support of new product development. He has contributed to several Investigational New Drug Applications and New Drug Applications in addition to authoring clinical study results for publication. From 1989 to 2004, Paterno held several other clinical research positions at Bausch & Lomb including Manager, Internal Research Clinic; Senior Research Optometrist, Global Vision Care; and Interim Director, Clinical Management, Personal Products Research and Development, among others. Dr. Paterno holds a Bachelor of Arts in Biological Sciences from the State University of New York at Binghamton, a Bachelor of Science in General Sciences and a Doctor of Optometry degree from the Pennsylvania College of Optometry.
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