APLM - Apollomics, Inc. Comprehensive Stock Profile

One-Sentence Summary of Key Findings: Apollomics (APLM) is a small clinical-stage oncology biotech with a focused pipeline led by Phase 2 asset vebreltinib (APL-101), minimal revenue from partnerships, ongoing Nasdaq compliance challenges, highly volatile stock performance, and very limited Wall Street coverage reflecting its high-risk pre-commercial status.

Stock Performance and Company Financials

Stock Performance (Historical Context)

Interpretation: The outsized 1-year gains reflect recovery from lows amid clinical updates and financings, but the wide range and low volume indicate speculative trading rather than fundamental stability.

Limitation: Historical returns include effects of corporate actions (e.g., SPAC merger as Maxpro Capital Acquisition Corp.); past performance is not indicative of future results. Data as of mid-July 2026 snapshots.

Company Financials (TTM / Recent Periods)

MetricValueNotes
Revenue (TTM)$8.84 millionLikely licensing/milestone income (e.g., Asia rights deals); not product sales.
Net Income (TTM)-$10.94 millionOperating losses typical of clinical-stage biotech.
EPS (TTM, diluted)-$7.57High per-share loss due to low share count post-corporate actions.
Profit Margin-123.7%Deeply negative as expected pre-revenue.
Cash (most recent quarter)$3.28 millionLimited runway; supplemented by bridge financing.
Market Cap~$42–44 millionMicro-cap classification.
Return on Equity (TTM)-1,305%Extremely negative due to accumulated losses.
Return on Assets (TTM)-57.6%Inefficient asset utilization in R&D phase.

Recent Financial Highlights (from press releases)

Limitation/Assumption: Financial data primarily from Yahoo Finance and company press releases as of July 2026; full audited statements available in SEC filings (Form 20-F). No product revenue; sustainability depends on future partnerships, clinical success, or dilutive financings. Share count and EPS impacted by potential reverse splits or equity issuances common in this sector.

More Information: Yahoo Finance APLM | Company IR Site | Macrotrends Financials

Analyst Ratings

Consensus and Coverage

MetricDetails
Consensus RatingSell (based on 1 analyst)
Number of Analysts (last 12 months)1 (Weiss Ratings)
Recent ActionDowngrade to Sell (E+) on June 23, 2026
Price TargetsLimited/recently unavailable; older targets (2023) ranged ~$8.50 consensus with highs to $17

Uncertainty: Analyst coverage is extremely sparse; ratings can change rapidly with clinical data or financing news. No broad consensus from major firms.

Limitation: Data from MarketBeat and similar aggregators; always verify latest reports directly as coverage may be outdated or issuer-specific.

More Information: MarketBeat APLM Forecast | Yahoo Analyst Section

Customers and Competitors

Customers / Partners

Interpretation: Revenue is partnership-driven; success hinges on advancing pipeline to attract bigger pharma partners for global development/commercialization.

Competitors

Primary peers in oncology biopharma (MET inhibitors, immuno-oncology, AML/solid tumor focus):

CompanyTicker/Example FocusNotes
AbbVieABBVLarge-cap oncology leader with targeted therapies and IO.
AmgenAMGNEstablished player in targeted cancer treatments.
Gilead SciencesGILDStrong in oncology and antivirals with IO pipeline.
Vertex PharmaceuticalsVRTXPrecision medicine focus (though more cystic fibrosis historically).
RegeneronREGNIO and antibody expertise.
argenxARGXEmerging biotech with antibody platforms.
Smaller peerse.g., ARMP, BYSI, INMBSimilar micro-cap oncology or biotech plays.

Interpretation: APLM competes in a crowded oncology space where larger players have resources for combination therapies and global trials; differentiation relies on specific MET targeting and early IO assets.

Limitation: Competitor list is illustrative based on sector overlap; direct head-to-head clinical comparisons are limited. Market dynamics shift with new trial data or M&A.

More Information: Financhill Peer Comparison | Company Pipeline Page

Company Overview and History

Uncertainty: Clinical development success rates in oncology are historically low (~10–20% from Phase 1 to approval); partnership and funding outcomes are unpredictable.

Limitation: Pipeline status based on company disclosures and news up to mid-2026; always cross-reference latest clinicaltrials.gov or press releases for updates. No guarantee of future milestones.

More Information: Official Website | IR News Releases | Yahoo Company Profile