Crinetics Pharmaceuticals, Inc. (CRNX) FY2025 10-K Annual Report

Filed: Feb 26, 2026
Health Care
Pharmaceutical PreparationsSEC EDGAR

Crinetics Pharmaceuticals, Inc. (CRNX) 10-K annual report for fiscal year 2025, filed with SEC EDGAR on Feb 26, 2026. This page provides AI-powered analysis including business overview, management discussion & analysis (MD&A), risk factors, and key financial data such as revenue, net income, gross margin, operating margin, and return on equity (ROE) extracted from XBRL.

Crinetics Pharmaceuticals, Inc. FY2025 10-K Analysis

Business Overview

  • Core business: Discovery, development, commercialization of novel small molecule GPCR-targeted therapies for endocrine diseases and endocrine-related tumors
  • New product: FDA approved PALSONIFY (paltusotine) in September 2025, first once-daily oral treatment for acromegaly adults inadequately managed by surgery
  • Strategic shift: Launching focused U.S. commercial organization for PALSONIFY; expanding globally with EMA marketing authorisation expected H1 2026 and Japan licensing deal
  • Key metric: Pipeline includes 10+ disclosed programs; active enrollment in Phase 3 trials for paltusotine in Cushing’s syndrome; positive Phase 2 data on atumelnant with Phase 3 initiated
  • Noteworthy fact: PALSONIFY’s approval marks first oral, nonpeptide SST2R agonist for acromegaly, representing a novel therapeutic class and offering improved patient convenience

Management Discussion & Analysis

  • Revenue $7.7M in 2025 vs $1.0M in 2024, driven by $5.4M product sales from PALSONIFY launch
  • Operating margin -681.9% in 2025 vs -326.4% in 2024 (loss from ops $516.8M vs $338.9M on $7.7M vs $1.0M revenue)
  • Best segment: Collaboration revenue $2.3M up 119%, worst: operating expenses growth with SG&A up 92% to $191.3M
  • Cash, cash equivalents & investments $1.0B at end 2025 down 24%, raised $380M net in Jan 2026 equity offering, no dividends or buybacks
  • Outlook: Expects increasing product revenue but continued net losses; risks from R&D, commercialization costs, market acceptance, and global macro factors

Risk Factors

  • FDA approval risk: PALSONIFY regulatory compliance including U.S. FDA and EMA submissions with risk of delays or denial
  • Geopolitical risk: exposure to market disruptions from international conflicts including Russia-Ukraine and Middle East tensions
  • Supply chain risk: dependency on third-party manufacturers for clinical and commercial-scale production of PALSONIFY and other candidates
  • Competitive risk: potential market disruption if competitor therapies gain faster regulatory approval or wider physician acceptance
  • Financial risk: accumulated deficit $1.4B with reliance on $350M equity sales agreement for funding next 12 months

Crinetics Pharmaceuticals, Inc. FY2025 Key Financial Metrics
XBRL

Revenue

$8M

+640.7% YoY

Net Income

-$465M

-55.9% YoY

Operating Margin

-6714.8%

+2589870bp YoY

Net Margin

-6046.2%

+2267447bp YoY

ROE

-46.9%

-2438bp YoY

Total Assets

$1.1B

-21.5% YoY

EPS (Diluted)

$-4.95

-34.1% YoY

Operating Cash Flow

-$378M

-67.2% YoY

Source: XBRL data from Crinetics Pharmaceuticals, Inc. FY2025 10-K filing on SEC EDGAR. All figures in USD.

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