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Zenas BioPharma, Inc./$ZBIO

1D1W1M3M6MYTD1Y5YMAX

About Zenas BioPharma, Inc.

Zenas BioPharma Inc is a clinical-stage biopharmaceutical company. Its I&I product candidate, obexelimab, is a bifunctional monoclonal antibody designed to bind both CD19 and FcyRIIb, which are present across B cell lineage, in order to inhibit the activity of cells that are implicated in many autoimmune diseases without depleting them. The Company manages its operations on a consolidated basis as a single reportable segment focused on the research, development and commercialization of transformative immunology-based therapies.
Ticker
$ZBIO
Sector
Health
Primary listing
NASDAQ
Employees
167

ZBIO Metrics

BasicAdvanced
$1.9B
-
-$9.05
-1.02
-

What the Analysts think about ZBIO

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

Bulls say / Bears say

Phase 3 INDIGO cut the risk of an IgG4-RD flare by 56% versus placebo, and significantly improved remission and other key outcomes. This gives obexelimab a strong late-stage clinical evidence base. (New England Journal of Medicine)
Obexelimab reduced rescue-steroid use and steroid-related toxicity; in the open-label extension, the estimated 12-month probability of remaining flare-free was 93% by investigator and adjudication-committee assessment. These findings support its potential as a longer-term, steroid-sparing treatment. (BioSpace)
The FDA accepted the obexelimab application and set 27 May 2027 as its target decision date. That puts Zenas on a defined path towards a possible first product launch and gives investors a clear regulatory catalyst. (SEC)
Obexelimab reduced flare risk by 56%, below the 87% reduction reported for Uplizna in its separate pivotal trial. The studies were not head-to-head, but the gap raises questions about obexelimab’s differentiation against an established treatment. (Stockopedia)
Hypersensitivity was reported in 16.5% of obexelimab-treated patients versus 11.3% on placebo in INDIGO. Although serious adverse events were less common with obexelimab overall, this higher rate could be a tolerability concern. (New England Journal of Medicine)
Zenas reported a $111.5 million second-quarter net loss and says its runway to the second quarter of 2029 assumes approval-linked funding, including a $75 million royalty payment and a $75 million debt draw. Delayed or denied approval could therefore weaken its funding outlook and increase pressure to raise capital. (SEC)
Data summarised monthly by Lightyear AI. Last updated on 20 Oct 2026.

ZBIO Financial Performance

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

ZBIO 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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