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Roth says NALIPIFOX approval gives investors optimism for Panbela SBP-101 trial

Roth MKM analyst Jonathan Aschoff notes that on Tuesday, Ipsen (IPSEY) received FDA approval in first-line mPDAC for Onivyde in combination with 5-FU/leucovorin and oxaliplatin — NALIRIFOX. This approval is the first first-line FDA approval in mPDAC since the mPACT trial that led to the 2013 approval of gemcitabine/Abraxane, which served as the control arm for Ipsen’s NALIRIFOX trial. The firm believes that the earlier Phase 1/2 results for NALIRIFOX in first-line mPDAC give investors reason for optimism for SBP-101’s pivotal trial when viewed in light of Panbela Therapeutics’ (PBLA) Phase 1/1b results in first-line mPDAC. Roth has a Buy rating on Panbela Therapeutics with a price target of $25 on the shares.

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