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Zevra Therapeutics/$ZVRA

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About Zevra Therapeutics

Zevra Therapeutics Inc is a commercial-stage company with a late-stage pipeline committed to bringing life-changing therapeutics to people living with rare diseases. The Company is focused on expanding patient access, progressing its pipeline toward key milestones, and delivering meaningful outcomes for patients with unmet needs. The commercialization of its product, marketed in the United States for Niemann-Pick disease type C (NPC), a rare, progressive neurodegenerative disease, provides a corporate foundation and demonstrates its ability to advance therapies from development to market.
Ticker
$ZVRA
Sector
Health
Primary listing
NASDAQ
Employees
61

ZVRA Metrics

BasicAdvanced
$583M
11.12
$0.88
0.95
-

What the Analysts think about ZVRA

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

Bulls say / Bears say

MIPLYFFA is gaining commercial traction: Q2 2026 net sales rose 40% year on year to $30.2 million, helping lift total revenue 53% to $39.7 million. Operating expenses also fell year on year, supporting a path to stronger underlying profitability. (Zevra Therapeutics)
The balance sheet gives Zevra room to fund growth without an immediate financing need: it held $260.2 million in cash and investments at Q2 end and had repaid its term loan. Management said those resources were sufficient to execute its plans independently of capital markets. (Zevra Therapeutics, Zevra Therapeutics)
The US opportunity could extend beyond today’s diagnosed market: management estimates 350–900 potential NPC patients, compared with roughly 300–350 currently diagnosed. Zevra had received 184 MIPLYFFA prescription forms by the end of Q2, leaving scope for growth if diagnosis efforts reach more patients. (Investing.com, Zevra Therapeutics)
European expansion is uncertain after the EMA’s CHMP issued a negative opinion, saying efficacy had not been sufficiently demonstrated. Zevra has sought re-examination, but approval and the timing of any European sales remain unresolved. (Medscape, Zevra Therapeutics)
Revenue is concentrated in MIPLYFFA: it generated $30.2 million of Q2’s $39.7 million total, while OLPRUVA contributed only $0.2 million. Expanded-access reimbursements are less predictable, leaving results reliant on continued MIPLYFFA sales growth. (Zevra Therapeutics, StockNow)
The celiprolol Phase 3 trial for vascular Ehlers-Danlos syndrome has an uncertain timeline: by Q2 end, only three confirmed events had occurred, against 28 needed for interim analysis, and 66 of 150 planned patients were enrolled. A slow event rate could delay the programme’s next meaningful readout. (Zevra Therapeutics)
Data summarised monthly by Lightyear AI. Last updated on 27 Oct 2026.

ZVRA Financial Performance

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

ZVRA Earnings Performance

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

Funds containing ZVRA

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