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An open-label, exploratory, limited dose escalation study to evaluate the pharmacokinetics, safety and tolerability of gemcitabine hydrochloride oral formulation in subjects with malignant tumors. |
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Consulting or Advisory Role - Boehringer Ingelheim; Onyx; Sanofi |
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Research Funding - Abbvie (Inst); Amgen (Inst); AstraZeneca (Inst); Boehringer Ingelheim (Inst); Bristol-Myers Squibb (Inst); Celgene (Inst); Gilead Sciences (Inst); HERON (Inst); Incyte (Inst); Sanofi (Inst); Tesaro (Inst) |
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Research Funding - Astex Pharmaceuticals (Inst); Boehringer Ingelheim (Inst); Endocyte (Inst); Genentech (Inst); GlaxoSmithKline (Inst); Merck Serono (Inst); Takeda (Inst) |
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Stock and Other Ownership Interests - Can-Fite BioPharma; Dipexium |
Consulting or Advisory Role - Angstrom Pharmaceuticals; Berg Pharma; Can-Fite BioPharma; Cleave Biosciences; Gem Pharmaceuticals; Immune System Key; InnoPharma; Onconova Therapeutics; Phosplatin Therapeutics; Sanofi; Taiwan Liposome; Verastem |
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No Relationships to Disclose |
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Stock and Other Ownership Interests - InnoPharmax |
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Stock and Other Ownership Interests - InnoPharmax |
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Stock and Other Ownership Interests - InnoPharmax |
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No Relationships to Disclose |