Transposon Therapeutics receives ARPA-H award for TPN-101
The up to $22M funding supports studying TPN-101 to extend healthspan under the PROSPR program. It targets LINE-1 inhibition to slow aging-related diseases.
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Biotechnology company developing therapies for neurodegenerative and aging-related diseases
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In short: Transposon Therapeutics advanced TPN-101 through FDA Fast Track, ARPA-H funding, ADDF investment, and ALS platform inclusion.
The up to $22M funding supports studying TPN-101 to extend healthspan under the PROSPR program. It targets LINE-1 inhibition to slow aging-related diseases.
Plans Phase 2 trial in Q4 2025, building on positive PSP and ALS results. Advances in HEALEY ALS trial.
TPN-101 joins Phase 2/3 HEALEY ALS Platform Trial after promising Phase 2 results in C9orf72-related ALS.
TPN-101 reduced Vital Capacity decline by 50%, slowed ALS progression, lowered biomarkers. Plans Phase 3 for C9orf72-related ALS.
The FDA granted fast track designation to TPN-101, an investigational therapy for progressive supranuclear palsy, based on promising phase 2a study results.
SAN DIEGO, March 04, 2026 (GLOBE NEWSWIRE) -- Transposon Therapeutics, a biotechnology company developing therapies for the treatment of neurodegenerative and aging-related diseases, today announced...
Building on the positive results of Phase 2 clinical trials in PSP and ALS, Transposon plans to initiate a Phase 2 clinical trial of TPN-101...
News provided by Transposon Therapeutics May 28, 2025, 8:00 AM ET In the Phase 2 Study of TPN-101 in patients with C9orf72-related ALS, TPN-101 showed...
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