Safety and Efficacy Study of Tenalisib (RP6530) in Combination With Pembrolizumab in Relapsed or Refractory cHL
Terminated
Rhizen Pharmaceuticals SA
Phase 1
To characterize safety, tolerability and to establish the maximum tolerated dose (MTD) for
Tenalisib in combination with Pembrolizumab in patients with cHL.
Efficacy and Safety Study of Tenalisib (RP6530), a Novel PI3K δ/γ Dual Inhibitor in Patients With Relapsed/Refractory Indolent Non-Hodgkin's Lymphoma (iNHL)
Completed
Rhizen Pharmaceuticals SA
Phase 2
To assess the anti-tumor activity and safety of Tenalisib in patients with
relapsed/refractory indolent Non-Hodgkin's Lymphoma (iNHL),
Tenalisib has been evaluated as an investigational new drug in number of early clinical
studies in patients with relapsed/refractory hematological malignancies and demonstrated
acceptable safety and promising efficacy in these patients. Since these advanced
relapsed/refractory patients have limited therapeutic options, it is reasonable to continue
Tenalisib in responding patients post completion of their participation in previous clinical
studies.
Safety and Efficacy of Tenalisib (RP6530) in Combination With Romidepsin in Patients With Relapsed/Refractory T-cell Lymphoma
Completed
Rhizen Pharmaceuticals SA
Phase 1/Phase 2
To characterize safety, tolerability and to establish the maximum tolerated dose (MTD) of
Tenalisib in combination with Romidepsin in patients with R/R T-cell lymphoma.
Efficacy and Safety of Tenalisib (RP6530) in Patients With Relapsed/Refractory Chronic Lymphocytic Leukemia (CLL)
Completed
Rhizen Pharmaceuticals SA
Phase 2
The trial is a Phase II, open label, Simon's two stage study design to evaluate the efficacy
and safety of Tenalisib in patients with CLL who have relapsed or are refractory after at
least one prior therapy.
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