Ligand Pharmaceuticals has reported that its Captisol-enabled, propylene glycol-free (PG-free) melphalan drug met all the endpoints in patients with multiple myeloma.
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The Phase II study included comparison of the safety, tolerability and pharmacokinetic profiles of PG-free melphalan intravenous formulation to the standard multiple myeloma treatment.
The Captisol-enabled drug is said to provide longer administration durations and slower infusion rates, enabling clinicians to safely achieve a higher dose intensity of pre-transplant chemotherapy.
The trial was conducted in partnership with The University of Kansas Cancer Center was partially funded by the Kansas Bioscience Authority.
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