Biotech entity
AMT-130 is the most frequent co-covered peer, appearing in 3 of the 3 tracked stories. gene-therapy accounts for 2 of the 3 tracked stories, while 1 other category carries the remainder. Source depth averages 2 original sources per story, versus 3.7 across the same-window beat baseline.
Last mentioned: Aug 5, 2026
Entity pulse
Coverage balance Positive coverage leads. Positive coverage exceeds negative coverage by 33 percentage points.
Figures are computed live from our source-verified story record — see our methodology for how impact and sentiment are derived.
AMT-130 is the most frequent co-covered peer, appearing in 3 of the 3 tracked stories. gene-therapy accounts for 2 of the 3 tracked stories, while 1 other category carries the remainder. Source depth averages 2 original sources per story, versus 3.7 across the same-window beat baseline. That works out to roughly 0.1 stories per week across a 156-day span. Their average consequence score of 5.7 runs below the beat's 6.2 for that window. This profile follows 3 Biotech stories mentioning uniQure across the period from March 3, 2026 to August 5, 2026.
Computed from the 3 stories linked to this entity, with beat comparisons drawn from all 551 Biotech stories published in the same date window. Shares are omitted below five stories and comparisons below a twenty-story baseline.
Coverage cohort
Other entities that clear the same relevance threshold in stories also covering uniQure. Shared-story counts are live from our verified record — not editorial picks.
Four-Year Follow-Up Data from AMT-130 Pivotal Study
Durability of gene therapy effect expected to be reported, a key factor for regulatory decisions.
Regulatory Submissions for AMT-130 in Huntington's Disease (Planned)
uniQure aims to file for U.S. and U.K. approval in Q3 2026, targeting accelerated pathways.
AMT-260 Preliminary Data and AMT-191 Further Analyses
Six-month follow-up from the Phase I/IIa AMT-260 trial in epilepsy and new Fabry data presented.
FDA Type B Meeting
Planned follow-up meeting to define the Phase III pathway for AMT-130 in Huntington's disease.
Earnings Release
Company announces 2025 results and provides update on FDA Type A meeting.
Updated AMT-191 Phase I/II Data in Fabry Disease
Interim data demonstrate sustained enzyme activity and safety in Fabry disease patients.
AMT-260 Data
Clinical data expected from the Phase I/IIa study in refractory mesial temporal lobe epilepsy.
Fiscal Year End
uniQure closes 2025 with $622.5M in cash and equivalents.
Positive Topline Data for AMT-130 in Huntington's Disease
uniQure reports positive pivotal Phase I/II data, showing statistically significant improvements in disease markers.
uniQure's AMT-130 for Huntington's disease is on track for U.S. and U.K. regulatory filings in Q3 2026, following positive pivotal data. Pipeline updates for AMT-191 and AMT-260 in Fabry disease and epilepsy show a broadening gene therapy platform.
Source: rttnews.com · finanzen.ch
uniQure’s AMT-130 update validates its gene therapy platform, while NTHI’s NEO212 advancement and an acquisition deal spotlight a busy week for biotech pipelines and dealmaking.
Source: Prabha Kurup (us) · Prabha Kurup (us)
uniQure reported a robust $622.5 million cash position, extending its operational runway into late 2029. While clinical data for its Huntington’s disease candidate AMT-130 remains strong, the company is still seeking regulatory alignment with the FDA on a definitive Phase III pathway.
uniQure is linked from 3 stories on this site, each scored at or above our 35% relevance threshold — see how these pages are built.
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