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Prothena/$PRTA

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About Prothena

Prothena Corp PLC is a late-stage clinical biotechnology company that focuses on protein dysregulation and a pipeline of investigational therapeutics with the potential to change the course of devastating neurodegenerative and rare and peripheral amyloid diseases. Prothena is developing and applying its proprietary CYTOPE technology to target a broad spectrum of intracellular disease pathways in the brain and periphery. The company's pipeline includes both wholly-owned and partnered programs like Prasinezumab, Coramitug (PRX004), BMS-986446 (PRX005), PRX019, TDP-43 CYTOPE, and PRX012-TfR, being developed for the potential treatment of Parkinson's disease, ATTR amyloidosis with cardiomyopathy, Alzheimer's disease, Amyotrophic lateral sclerosis (ALS), and other neurodegenerative diseases.
Ticker
$PRTA
Sector
Health
Primary listing
NASDAQ
Employees
67
Headquarters
Dublin, Ireland

Prothena Metrics

BasicAdvanced
$435M
-
-$0.83
-0.35
-

What the Analysts think about Prothena

Analyst ratings (Buy, Hold, Sell) for Prothena stock.
Analyst projections of the future price of Prothena stock.

Bulls say / Bears say

Roche’s Phase 2b PADOVA results showed exploratory clinical and biological signals that were consistent across clinical and biomarker measures. The findings support taking prasinezumab into Phase 3, although they do not yet prove it works. (BioSpace)
Coramitug has FDA Fast Track status and is being tested in a large Phase 3 study for ATTR cardiomyopathy. Earlier Phase 2 results showed improvement in a heart-failure biomarker and several measures of heart function, giving the programme clinical support beyond its disease rationale. (BioSpace)
Prothena ended Q2 with $289.1 million in cash and expects only $18–23 million of net cash use from operations and investing for 2026. This gives it a substantial buffer while partners advance its clinical programmes. (Last10K)
The PADOVA findings were described as exploratory, so they are not conclusive evidence that prasinezumab changes Parkinson’s disease progression. The ongoing Phase 3 trial still has to establish whether the signal translates into a clear clinical benefit. (BioSpace)
Prothena’s Phase 1 results for its wholly owned Alzheimer’s antibody PRX012 showed higher rates of ARIA-E, a brain-swelling safety issue, than approved anti-amyloid antibodies. That could limit how suitable the drug is for patients, despite its ability to reduce amyloid plaque. (MarketScreener)
Prothena has little current revenue to cushion delays: Q2 revenue was $1.01 million and it still reported an $18.6 million loss. Its two largest partnered Phase 3 programmes are not expected to reach primary completion until 2029, leaving years before pivotal results could validate them. (Simply Wall St, City A.M.)
Data summarised monthly by Lightyear AI. Last updated on 9 Oct 2026.

Prothena Financial Performance

Revenues and expenses
Income statement
QuarterlyAnnual
Q3 24
QoQ growth
Revenue
Net income
Profit margin

Prothena Earnings Performance

Company profitability
Earnings per share
QuarterlyAnnual
Q4 23
Q1 24
Q2 24
Q3 24
Q4 24
Actual
Expected
Surprise
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