Skip to main content
CSTLNasdaq

Castle Biosciences Inc.

·Friendswood, TX, United States·CEO: Mr. Derek J. Maetzold

CSTL evidence brief

What we can confirm

No verified snapshot fields are available yet.

What it means

The company data is ready for cross-source review; unsupported conclusions remain unknown.

What to watch

Watch the next source-backed data update.
BioSniper AIPage evidence connected

Prepared research question

What matters most for CSTL—catalysts, financial risk and supporting evidence?

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · CSTL

Castle Biosciences Inc. is a diagnostics company focused on providing genomic tests for dermatologic cancers, with a pipeline that includes gene therapies for rare diseases.

Key risk: Medicare coverage loss

5.9/10

BioSniper Score

Based on 4 of 6 signals

Market Cap

$1.02B

Cash Runway

Lead Asset

Financial data as of Jun 30, 2026.

Tracking 3 clinical trials · 2 catalysts for Castle Biosciences Inc..

AI OverviewAI overview is shown in English only.

Castle Biosciences Inc. is a diagnostics company focused on providing genomic tests for dermatologic cancers, with a pipeline that includes gene therapies for rare diseases.

  • Cash & equivalents of $62.1M as of 2026-06-30 [sec].
  • Total revenue of $103.5M as of 2026-06-30 [sec].
  • Net loss of $2.1M as of 2026-06-30 [sec].
  • Shareholders' equity of $470.9M as of 2026-06-30 [sec].
  • Total debt of $13.0M as of 2026-06-30 [sec].

What works

  • The company has a portfolio of commercial products generating revenue, with total revenue of $103.5M as of 2026-06-30 [sec].
  • Management believes existing cash, marketable securities, and anticipated product sales will fund operations for at least the next 12 months [sec_mda · as of 2026-07-30].
  • The company is investing in R&D and clinical studies to support current and future product candidates, indicating a commitment to pipeline growth [sec_mda · as of 2026-07-30].

What to weigh

  • The company lost Medicare coverage for its DecisionDx-SCC test in April 2025, which has reduced revenues and cash inflows, with further reductions expected unless reconsideration requests are approved [sec_mda · as of 2026-02-26].
  • Net income may fluctuate significantly from period to period, and the company expects expenses to increase substantially over time as it invests in commercialization and development activities [sec_mda · as of 2026-07-30].
  • The company's ability to maintain profitability heavily depends on maintaining Medicare coverage for its marketed products and successful commercialization of future products [sec_mda · as of 2026-02-26].

From the filings

Quoted directly from source documents.

  • Management expects existing cash and product sales to fund operations for at least 12 months.

    We believe that our existing cash and cash equivalents, marketable investment securities and anticipated cash generated from the sale of our commercial products will be sufficient to fund our operations for at least the next 12 months.

    SEC MD&A · May 6, 2026

  • Net income may fluctuate significantly and expenses are expected to increase.

    Our net (loss) income may fluctuate significantly from period to period, depending on the timing of our planned development activities, the growth of our sales and marketing activities and the timing of revenue recognition under ASC 606. We expect our expenses will increase substantially over time as we: • execute clinical studies to generate evidence supporting our current and future product candidates; • execute our commercialization strategy for our current

    SEC MD&A · July 30, 2026

Catalyst timeline

  • 2037-07-01 · Phase3_Topline · fcx-007 — Phase 3 Topline: A Pivotal Phase 3 Study of FCX-007 (Genetically-Modified Autologous Human Dermal Fibroblasts) for ReTopline results from a pivotal Phase 3 study of FCX-007, a gene therapy for a rare disease, are expected; data will inform potential regulatory submission.
  • 2042-02-01 · Phase3_Topline — Phase 3 Topline: Evaluation of Dabocemagene Autoficel (D-Fi; FCX-007; Genetically Modified Autologous Human Dermal FiTopline results from a Phase 3 study evaluating dabocemagene autoficel (FCX-007) are expected; this is a later-stage readout for the same gene therapy candidate.
Risks & what to watch (4)

Key risks

  • Medicare coverage lossLoss of Medicare coverage for DecisionDx-SCC test in April 2025 has reduced revenues and cash inflows; further reductions expected unless reconsideration requests are approved [sec_mda · as of 2026-02-26].
  • Profitability dependenceAbility to maintain profitability heavily depends on maintaining Medicare coverage for marketed products and successful commercialization of future products [sec_mda · as of 2026-02-26].
  • Expense growthExpenses are expected to increase substantially over time as the company invests in clinical studies, commercialization, and pipeline development [sec_mda · as of 2026-07-30].
  • Cash runway uncertaintyCash runway estimates are based on assumptions that may prove wrong, potentially depleting capital resources sooner than expected [sec_mda · as of 2026-07-30].

What to watch

  • Outcome of reconsideration requests for Medicare coverage of DecisionDx-SCC test [sec_mda · as of 2026-02-26].
  • Progress and results of clinical studies for pipeline products, including gene therapy candidates [sec_mda · as of 2026-07-30].
  • Revenue trends from commercial products and ability to maintain or grow market access [sec_mda · as of 2026-07-30].

Sources: SEC MD&A · Generated August 29, 2026 · How we verify sources →

Run Castle Biosciences Inc. through your own thesis

Use the pipeline, catalyst, financial, FDA, and market facts on this page as inputs to a protocol you control.

Your protocol can:

  • Turn available Castle Biosciences Inc. facts into screen rules or deeper checks
  • Show cited findings, blockers, and unresolved evidence together
  • Save the logic and rerun it as the company evidence changes
Run a thesis on this company — freeRun a thesis on this company

Evidence & data

Score breakdownBased on 4 of 6 signals · derived from public data

No clinical pipeline tracked — this score reflects financial & catalyst signals only.

Cash Runway10.0

Profitable (positive operating cash flow)

Financial Health9.7

D/E 0.19 · 0% dilution

Pipeline MaturityN/A

No tracked pipeline phase

Pipeline BreadthN/A

No tracked pipeline candidates

Catalyst Momentum4.0

2 upcoming, next in ~3958d

Insider Signal0.0

0 buys · 148 sells (180d)

Catalysts

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

185

Total value held

$633.3M

Showing top 10 of 185 institutional holders of Castle Biosciences Inc.. Open the full 13F history after sign-in.

Short Interest

as of May 20, 2026
% of float
4.8%
Days to cover
4.8
Shares short
1,429,016
Daily short volume
-

Short percent of float and days-to-cover reflect reported short positioning. Daily short volume is the exchange-reported short share of a single day's trading volume and is noisier. See the most-shorted biotech ranking →

CSTL short interest

Governance

Frequently asked questions

What is the AI investment thesis for Castle Biosciences Inc.?

Castle Biosciences Inc. is a diagnostics company focused on providing genomic tests for dermatologic cancers, with a pipeline that includes gene therapies for rare diseases.

What is Castle Biosciences Inc.'s next catalyst?

Castle Biosciences Inc.'s next tracked catalyst is a Phase3_Topline event — "Phase 3 Topline: A Pivotal Phase 3 Study of FCX-007 (Genetically-Modified Autologous Human Dermal Fibroblasts) for Re" — expected July 1, 2037.

Who is the CEO of Castle Biosciences Inc.?

Mr. Derek J. Maetzold is the chief executive officer of Castle Biosciences Inc. (CSTL).

Where is Castle Biosciences Inc. headquartered?

Castle Biosciences Inc. (CSTL) is headquartered in Friendswood, TX, United States.

925 companies232,681 SEC filings21,417 clinical trials100% citation-verification pass rate (7d)How we verify →

The AI overview and BioSniper Score are neutral, data-derived signals built from public SEC filings, ClinicalTrials.gov and FDA records — not investment advice.