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A multicenter, open label, phase II study to assess the efficacy and safety of APO866 in the treatment of patients with refractory or relapsed cutaneous T-cell lymphoma. |
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Consulting or Advisory Role - Bristol-Myers Squibb; Merck Sharp & Dohme |
Travel, Accommodations, Expenses - Bristol-Myers Squibb; Merck Sharp & Dohme; Roche Pharma AG |
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Travel, Accommodations, Expenses - St. Jude Medical (I) |
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No Relationships to Disclose |
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Travel, Accommodations, Expenses - Amgen |
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No Relationships to Disclose |
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Consulting or Advisory Role - Teva |
Travel, Accommodations, Expenses - Cephalon; Johnson & Johnson; Teva; Therakos |
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Honoraria - Bristol-Myers Squibb; GlaxoSmithKline; Roche Pharma AG |
Consulting or Advisory Role - Bristol-Myers Squibb; GlaxoSmithKline; Roche Pharma AG |
Travel, Accommodations, Expenses - Bristol-Myers Squibb; GlaxoSmithKline; Roche Pharma AG |
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No Relationships to Disclose |
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Consulting or Advisory Role - Affimed Therapeutics; Amgen; Novartis; Roche Pharma AG; Teva |
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Honoraria - Bristol-Myers Squibb; GlaxoSmithKline; MSD; Novartis; Roche |
Consulting or Advisory Role - Bristol-Myers Squibb; GlaxoSmithKline; MSD; Novartis; Roche |
Research Funding - Bristol-Myers Squibb; GlaxoSmithKline; MSD; Novartis; Roche |