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Nventa presents additional positive data from Phase I neoplasia trial

Nventa Biopharmaceuticals has announced positive immunological data from the third cohort of its ongoing Phase I clinical trial of its lead product candidate, HspE7, in patients with cervical intraepithelial neoplasia, a precursor to cervical cancer.

HPV 16 E7-specific T-cell responses were elicited in all four subjects in the study’s third cohort following administration of 500mcg of HspE7 and 1,000mcg of Poly-ICLC, a potent toll-like receptor 3 (TLR-3) adjuvant. All T-cell responses represented significant changes from baseline, indicating that the responses were a direct result of treatment with HspE7.

Gregory McKee, president and CEO of Nventa, said: “We continue to be very encouraged with the immunological results from our Phase I HspE7 trial as they demonstrate that administration of HspE7 induces T-cell responses that we believe to be therapeutic. These positive immunological data, along with the safety data analyzed to date, provide a strong foundation for our Phase II trial expected to begin mid-2008.”