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Pamolen is a PARP inhibitor combination therapy being developed by Alessa Therapeutics for the treatment of intermediate to high-risk localized prostate cancer. The therapy utilizes a combination regimen of small molecule PARP inhibitors designed to block PARP-mediated DNA repair through the inhibition of Poly [ADP-ribose] polymerase (PARP). A distinguishing feature of Pamolen is its delivery method, which involves implantable subcutaneous drug delivery devices designed for the extended release of the medication directly to prostate tissue. This localized approach is intended to provide high concentrations of the drug at the tumor site while reducing systemic exposure and associated side effects. As of 2024, the program is in the IND-enabling phase, with an IND filing anticipated in the second half of 2026.
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