Welcome to our dedicated page for Castle Biosciences news (Ticker: CSTL), a resource for investors and traders seeking the latest updates and insights on Castle Biosciences stock.
Castle Biosciences, Inc. (Nasdaq: CSTL) is a diagnostics company focused on molecular tests that guide patient care in dermatologic and gastroenterological disease. The CSTL news feed highlights company announcements, clinical data, financial results and corporate updates that shape how investors and clinicians view its role in precision medicine.
Readers can follow news on Castle’s core test portfolio, including DecisionDx-Melanoma for cutaneous melanoma, TissueCypher Barrett’s Esophagus, DecisionDx-SCC for high-risk cutaneous squamous cell carcinoma, MyPath Melanoma and its suite of tests for uveal melanoma such as DecisionDx-UM, DecisionDx-PRAME and DecisionDx-UMSeq. Coverage also includes updates on AdvanceAD-Tx, the company’s gene expression profile test designed to guide systemic treatment decisions in moderate-to-severe atopic dermatitis.
In addition to product and clinical evidence updates, CSTL news items feature quarterly and annual financial results, test volume trends for core revenue drivers, and guidance ranges reported in earnings releases. Regulatory and corporate governance developments, such as bylaw amendments disclosed in Form 8-K filings, as well as participation in healthcare and investor conferences, are also common topics.
Because Castle Biosciences emphasizes rigorous clinical validation, many news releases center on new studies, meta-analyses and expert consensus papers that evaluate the performance of its tests in real-world and prospective cohorts. These articles provide insight into how DecisionDx-Melanoma, TissueCypher and other assays are being integrated into clinical decision-making.
For investors, clinicians and researchers tracking CSTL, this news page offers a centralized view of earnings announcements, product launches, reimbursement developments, clinical data presentations and corporate events related to Castle Biosciences’ molecular diagnostics business.
Castle Biosciences (Nasdaq: CSTL) will present research data on its dermatologic gene expression profile (GEP) tests at the 2025 Winter Clinical Dermatology Conference in Hawaii. The company will showcase three posters focusing on different tests:
1. DecisionDx-Melanoma: Research on i31-SLNB's ability to identify melanoma patients with low risk of SLN positivity
2. DecisionDx-SCC: Study on using 40-GEP test to identify high-risk immunosuppressed patients with cutaneous squamous cell carcinoma
3. MyPath Melanoma: Research on enabling access to prognostic GEP testing for invasive melanoma
The posters will be displayed in the Queen's Ballroom 5-6 throughout the conference, with additional information available at Castle's exhibit hall booth.
Castle Biosciences (CSTL) has announced it will release its fourth quarter and full-year 2024 financial results after market close on Thursday, February 27, 2025. The company will host a conference call and webcast at 4:30 p.m. Eastern time to discuss the results.
Investors can access the live webcast through the company's Investor Relations page or directly via the provided link. For those joining by phone, the U.S. dial-in number is 1-833-470-1428 with access code 944585. International dial-in numbers are available through a separate link. A Q&A session will follow management's presentation, and a webcast replay will be available after the call.
Castle Biosciences (CSTL) will present data on its dermatologic portfolio at Maui Derm Hawaii 2025, with its DecisionDx-SCC poster selected as a top five finalist for the Akamai Award. The study, involving 1,408 patients with cutaneous squamous cell carcinoma (SCC), demonstrates improved risk stratification when combining test results with BWH staging.
The DecisionDx-SCC test showed significant metastasis prediction capabilities with three-year metastasis-free survival rates of 92.3% for Class 1, 81.3% for Class 2A, and 57.8% for Class 2B. Additional studies showed DecisionDx-Melanoma reduced unnecessary SLNB procedures by 25%, while MyPath Melanoma research revealed 24% diagnostic discordance among dermatopathologists for difficult-to-diagnose melanocytic lesions.
Castle Biosciences (CSTL) announced preliminary unaudited results for Q4 and full-year 2024, expecting to meet or exceed the top end of its guided revenue range of $320-330 million, representing at least 50% growth over 2023. The company delivered 96,071 total test reports in 2024, up 36% from 2023.
Q4 2024 saw 24,071 test reports delivered, a 19% increase year-over-year. Notable growth was seen in TissueCypher Barrett's Esophagus tests (+94%) and DecisionDx-SCC (+22%), while MyPath Melanoma and IDgenetix tests decreased by 14% and 5% respectively.
The company's year-end 2024 financial position shows approximately $293 million in combined cash, cash equivalents, and marketable investment securities. However, Novitas, a Medicare Administrative Contractor, finalized a non-coverage determination for the DecisionDx-SCC test on January 9, 2025.
Castle Biosciences (CSTL) has received assay approval from the New York State Department of Health for its TissueCypher Barrett's Esophagus test. This approval marks the completion of New York state approval for all of Castle's tests across its dermatology, gastroenterology and ophthalmology portfolios, as well as its clinical laboratories in Phoenix and Pittsburgh.
TissueCypher is the first AI-driven precision medicine test designed to predict progression risk from Barrett's esophagus (BE) to esophageal cancer. The test analyzes cancer-associated biomarkers and spatial biology features to identify molecular signatures of BE progression before visible tissue changes occur. This tool helps clinicians risk-stratify the estimated 5% of U.S. adults with BE, enabling risk-aligned surveillance or earlier interventions to prevent cancer development.
Castle Biosciences (CSTL) provided an update on its pipeline test for moderate-to-severe atopic dermatitis (AD) patients seeking systemic treatment. Preliminary data shows the test may identify patients likely to achieve a super response (90% or greater reduction in EASI score) to targeted therapies within three months.
The company has enrolled over 1,100 patients across 39 clinical study sites for its development and validation study. With an estimated 6 million U.S. patients diagnosed with moderate-to-severe AD annually, and approximately 760,000 seeking systemic treatment, the test aims to improve the current 'trial-and-error' approach, where 25% of patients discontinue initial therapy and 50% show persistent disease burden.
Assuming successful validation, Castle expects to launch the test by the end of 2025.
Castle Biosciences (CSTL) announced that its Board of Directors' Compensation Committee has granted restricted stock units (RSUs) to 135 employees, covering 173,542 shares of common stock. The grants were made under the Company's 2022 Inducement Plan, complying with Nasdaq Listing Rule 5635(c)(4). The RSUs have a four-year vesting schedule, with 25% vesting after the first year and the remaining balance vesting in three equal annual installments, contingent on continued employment.
Castle Biosciences (CSTL) announced the publication of an independent meta-analysis in Cancers evaluating their DecisionDx-Melanoma test for predicting melanoma patient outcomes. The analysis, reviewing 13 peer-reviewed studies, confirms the test's effectiveness in risk stratification for cutaneous melanoma (CM) patients.
The study revealed five-year melanoma-specific survival rates of 99.8% for lowest risk (Class 1A), 97.6% for increased risk (Class 1B/2A), and 83.4% for highest risk (Class 2B) patients. The test demonstrated consistent ability to stratify patients into risk groups with significantly different outcomes, supporting its use alongside current staging systems for enhanced patient care management.
Castle Biosciences (Nasdaq: CSTL), a healthcare company specializing in innovative diagnostic tests, has announced its participation in the Piper Sandler 36th Annual Healthcare Conference. The company's executive management will deliver a corporate overview on Wednesday, Dec. 4, 2024, at 10:50 a.m. Eastern time.
A live audio webcast of the presentation will be accessible through Castle Biosciences' investor relations website. Additionally, a replay of the presentation will be made available after the live broadcast concludes.
Castle Biosciences (CSTL) has been named a Houston Top Workplace for 2024 by the Houston Chronicle, marking its fourth consecutive year receiving this recognition. The company also earned three additional Culture Excellence awards for Employee Appreciation, Employee Well-Being, and Professional Development.
The recognition is based on anonymous employee feedback collected through Energage's third-party survey, which measures various aspects of employee experience including feeling respected, supported, and empowered. Castle has accumulated a total of 12 Top Workplaces awards for 2024, including regional awards for Houston and Arizona, and ten national awards. The company ranked 28th among 370 companies in the Top Workplaces USA category and fourth out of 95 firms in the Healthcare Industry category.