Pliant Therapeutics, Inc. PLRX launched on Monday knowledge from the primary three of 5 potential cohorts of its ongoing Section 1 dose escalation trial of PLN-101095, together with Merck & Co Inc.’s MRK Keytruda (pembrolizumab), in sufferers with immune checkpoint inhibitor (ICI)-refractory superior or metastatic strong tumors.
Interim outcomes demonstrated PLN-101095 antitumor exercise together with pembrolizumab, with three partial responses noticed in cohort three on the 1000 mg administered orally twice every day (BID) dose, representing a 50% goal response fee (ORR) on the highest dose examined so far.
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PLN-101095 was typically effectively tolerated throughout all doses examined.
9 sufferers with six totally different tumor sorts had been enrolled in cohorts one by way of three of the trial.
Sufferers had been handled for 14 days with PLN-101095 at doses of 250 mg, 500 mg or 1000 mg administered orally BID, adopted by therapy with a mix of PLN-101095 and pembrolizumab at 200 mg administered intravenously each three weeks (Q3W):
- Throughout all doses examined, PLN-101095 was typically effectively tolerated.
- Of the six sufferers handled on the 1000 mg BID dose of PLN-101095, three (50%) confirmed partial responses had been noticed. All three sufferers stay on therapy.
- Non-Small Cell Lung Most cancers (NSCLC): Confirmed partial response with a 74% discount in tumor dimension at Week 18; preliminary partial response was noticed at Week 10.
- Cholangiocarcinoma: Confirmed partial response with a 48% discount in tumor dimension at Week 42; preliminary partial response was noticed at Week 34.
- Melanoma: Confirmed partial response with a 42% discount in tumor dimension at Week 27; preliminary partial response was noticed at Week 18.
The Section 1 trial of PLN-101095 is at the moment enrolling the fourth of 5 potential cohorts. The fourth cohort is evaluating PLN-101095 at 1000 mg, 3 times every day (TID).
PLRX Value Motion: Pliant Therapeutics inventory is up 12.99% at $1.74 at publication Monday.
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