FDA Approval of investigation drug triphendiol

Discussion Board Forums Clinical Trials FDA Approval of investigation drug triphendiol

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  • #25454
    marions
    Moderator

    I had contacted the principal investigator in re: to the Phase II study conducted with this drug. Previously, Cholangiocarcinoma had been targeted however, the current Phase II clinical trial only mentioned Pancreatic Cancer.
    I received an immediate response to my question:

    You are correct that some time back we did announce that Triphendiol might potentially benefit Cholangiocarcinoma patients. Its potential to be used in this indication is undiminished and we are confident that it could be equally effective in cholangiocarcinoma as it seems to be in pancreatic cancer and we continue to pursue this indication in pre-clinical studies. However to simplify the clinical development program towards registration we have decided to target pancreatic cancer in our Phase II trials. Should we achieve registration for this indication the drug could be used

    #25453
    marions
    Moderator

    After contacting the Group Director of Research (Prof. J. Husband) of Marshall Edwards Inc. (an Australian company) in re: to the beginning date of this clinical trial, I have been informed that a start date for the trial approved under this IND has not been set. The Principal Investigator is:

    Dr. Wasif Saif
    Yale University School of Medicine
    Section of Medical Oncology
    333 Cedar Street, FMP 116
    New Haven, CT 06520
    United States of America
    Bus: +1 (203) 737-1569
    Bus Fax: +1 (203) 737-2617

    #1895
    rank
    Member

    Came across this and thought some might be interested

    Jan 08, 2009 (M2 EQUITYBITES via COMTEX) — MSHL | Quote | Chart | News | PowerRating — Marshall Edwards Inc (NasdaqGM:MSHL), a specialist oncology company focused on the clinical development of novel anti-cancer therapeutics, said on 7 January that the company has received Investigative New Drug (IND) approval from the United States Food and Drug Administration (FDA) to undertake clinical studies with triphendiol as a chemosensitising agent in combination with gemcitabine.

    The company stated that the approval will allow a Phase Ib study of triphendiol in combination with gemcitabine in patients with unresectable, locally advanced or metastatic pancreatic and bile duct cancers. A Triphendiol (NV-196) is an investigational drug, currently being developed as an orally-delivered chemosensitising agent, intended for use in conjunction with standard chemotoxic anti-cancer drugs for the treatment of late stage pancreatic cancer, cholangiocarcinoma and melanoma.

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