IDEAYA Biosciences, Inc.

IDEAYA Biosciences, Inc.

IDYA
IDEAYA Biosciences, Inc.US flagNASDAQ Global Select
27.87
USD
-1.07
- -
2.45BMarket Cap
2017 Y
2018 Y
2019 Y
2020 Y
2021 Y
2022 Y
2023 Y
2024 Y
2025 Y
TTM
Revenue per Share
- -
- -
- -
0.79
0.79
1.23
0.41
0.09
2.47
2.54
Basic EPS, GAAP
-0.83
-2.41
-3.36
-1.4
-1.41
-1.42
-1.96
-3.36
-1.28
-1.58
Free Cash Flow per Basic Share
-0.98
-2.06
-3.25
2.22
-1.66
-2.19
-2.04
-3.08
-0.83
-0.99
Dividend per Share
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
Book Value per Share
-1.14
-3.55
-7.4
-5.14
-5.01
-5.68
-6.06
-7.63
-8.32
-9.43
Tangible Book Value per Share
-1.11
-3.44
8.03
8.02
8.55
8.43
10.8
12.97
11.56
10.58
Basic Weighted Avg Shares
14
14
12
25
35
41
58
82
88
89
Sales/Revenue/Turnover
- -
- -
- -
20
28
51
23
7
219
225
Operating Margin (%)
- -
- -
- -
-180.9
-179.91
-122.72
-574.85
-4,671.07
-72.84
-81.44
Depreciation Expense
- -
1
1
1
3
4
4
4
5
5
Net Income, GAAP
-12
-34
-42
-34
-50
-59
-113
-274
-114
-140
Effective Tax Rate (%)
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
Profit Margin (%)
- -
- -
- -
-176.55
-178.1
-115.17
-483.05
-3,921.1
-51.99
-62.17
Working Capital
11
85
95
250
206
339
506
644
608
631
LT Debt
- -
- -
6
5
3
2
1
19
28
28
Total Equity
-16
-49
100
198
302
349
621
1,059
1,023
937
Return on Invested Capital (%)
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
Return on Capital (%)
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -
Return on Common Equity (%)
- -
- -
- -
- -
- -
- -
- -
- -
- -
- -

Capital Structure

FRC

in mil. unless spec.
Sep'25
Dec'25
Mar'26
ST Debt
- -
- -
- -
LT Borrowings
- -
- -
- -
LT Finance Leases
27
28
28
Preferred Equity and Hybrid Capital
- -
- -
- -
Shares Outstanding
88
88
88
Market Capitalization
2,399
3,059
2,951

Working Capital

FRC

in mil. unless spec.
Sep'25
Dec'25
Mar'26
Total Current Assets
803
667
696
Cash, Cash Equivalents & STI
787
639
671
Accounts Receivable, Net
- -
- -
- -
Inventories
- -
- -
- -
Total Current Liabilities
65
59
65
Payables & Accruals
64
58
64
ST Debt
- -
- -
- -
Deferred Revenue
- -
- -
- -

Growth Rates

FRC

in mil. unless spec.

(avg. rate of change)

10 years
5 years
1 year
Total Equity
- -
42.56%
-3.42%
Free Cash Flow
- -
-15.67%
-70.78%
Net Income, GAAP
- -
47.82%
-58.58%
Sales/Revenue/Turnover
- -
605.11%
3,024.43%
Total Cash Common Dividend
- -
- -
- -

Quarterly Revenue

FRC

in mil. unless spec.

Year

Q1
Q2
Q3
Q4
FY
2024
- -
- -
- -
7
7
2025
- -
- -
208
11
219
2026
7
- -
- -
- -
- -

Quarterly Earnings Per Share

FRC

in mil. unless spec.

Year

Q1
Q2
Q3
Q4
FY
2024
-0.55
-0.68
-0.6
-1.49
-3.36
2025
-0.82
-0.88
1.35
-0.94
-1.28
2026
-1.11
- -
- -
- -
- -

Quarterly Dividends Per Share

FRC

in mil. unless spec.

Year

Q1
Q2
Q3
Q4
FY
2024
- -
- -
- -
- -
- -
2025
- -
- -
- -
- -
- -
2026
- -
- -
- -
- -
- -

Company Description

APIChat
CEO
Yujiro S. Hata
Full Time Employees
131
Sector
Healthcare
Industry
Biotechnology
Address
7000 Shoreline Court South San Francisco CA United States of America 94080
IPO Date
May 23, 2019
Business
IDEAYA Biosciences, Inc. is a clinical-stage precision medicine oncology company focused on the discovery, development, and commercialization of targeted therapeutics principally in precision oncology. The company’s core product pipeline includes small-molecule drugs and antibody-drug conjugates (ADCs) centered around synthetic lethality and biomarkers-driven patient selection. Key products in clinical development include darovasertib (IDE196), a protein kinase C (PKC) inhibitor for tumors with GNAQ or GNA11 mutations such as uveal melanoma; IDE397, a methionine adenosyltransferase 2A (MAT2A) inhibitor targeting cancers with MTAP gene deletions; IDE161, a poly(ADP-ribose) glycohydrolase (PARG) inhibitor for tumors with homologous recombination deficiency (HRD); and IDE034, a bispecific B7H3/PTK7 TOP1 antibody-drug conjugate designed for solid tumors expressing these targets. IDEAYA employs integrated biomarker and small molecule drug discovery platforms and collaborates with leading pharmaceutical companies to advance its pipeline globally. The company operates primarily out of South San Francisco, California, and was founded to leverage synthetic lethality approaches to selectively target cancer vulnerabilities while sparing normal cells. Recent major corporate developments include strategic partnerships and collaborations with pharmaceutical companies such as GlaxoSmithKline (GSK), which focuses on IDEAYA’s synthetic lethality programs including MAT2A, Pol Theta, and Werner Helicase, with shared development costs and profit-sharing arrangements. Partnership with Gilead centers on the IDE397 program, and a collaboration with Pfizer supports development of darovasertib. Additionally, in September 2025, IDEAYA entered a global licensing and collaboration agreement with Servier, under which Servier obtained rights to darovasertib outside the U.S., bringing in $210 million upfront plus up to $320 million in milestones, expanding the commercial and clinical development reach of this program worldwide. In December 2025, the U.S. Food and Drug Administration cleared IDEAYA’s investigational new drug application for IDE034, initiating a Phase 1 clinical trial enrolling patients in the first quarter of 2026 targeting multiple solid tumors including lung, colorectal, head and neck, and ovarian cancers. These recent advances underscore IDEAYA’s commitment to advancing potentially first-in-class, precision-guided oncology therapies and expanding its clinical pipeline while strategically leveraging partnerships to enhance global development and commercialization efforts.

Company News

APIChat
  • IDEAYA Biosciences and Servier Provide Complete Data from Phase 2/3 Registrational OptimUM-02 Trial of the Darovasertib Combination in First Line HLA*A2:01 Negative Metastatic Uveal Melanoma in a Late

  • IDEAYA Biosciences and Servier Provide Complete Data from Phase 2/3 Registrational OptimUM-02 Trial of the Darovasertib Combination in First Line HLA*A2:01 Negative Metastatic Uveal Melanoma in a Late-Breaking Oral Presentation at ASCO

  • IDEAYA Biosciences Announces Inducement Grants under Nasdaq Listing Rule 5635(c)(4)

  • IDEAYA Biosciences Announces Inducement Grants under Nasdaq Listing Rule 5635(c)(4)

  • IDEAYA Biosciences Spotlights Darovasertib Win, FDA Review Path at Oncology Summit

  • IDEAYA Biosciences Announces Participation at the 2026 Jefferies Global Healthcare Conference

  • IDEAYA Biosciences Eyes Busy 2026 as Darovasertib Advances Toward FDA Filing

  • B7-H3 Becomes The Hottest Antigen In Oncology, And One NK Engager Enters Clinic

  • IDEAYA Biosciences Says Melanoma Drug on Track for NDA After Strong Trial Data

  • IDEAYA Biosciences, Inc. (IDYA) Presents at Bank of America Global Healthcare Conference 2026 Transcript

  • IDEAYA Biosciences, Inc. (IDYA) Reports Q1 Loss, Misses Revenue Estimates

  • IDEAYA Biosciences Reports First Quarter 2026 Financial Results and Provides Business Update

  • IDEAYA Biosciences Announces Inducement Grants under Nasdaq Listing Rule 5635(c)(4)

  • IDEAYA Biosciences to Initiate New Drug Application Submission from the Darovasertib OptimUM-02 Trial under the Oncology Center of Excellence Real-time Oncology Review (RTOR) Program

  • IDEAYA Biosciences Announces Late-Breaking Abstract Oral Presentation at ASCO 2026 to Provide Complete Data from Phase 2/3 Registrational Trial (OptimUM-02) of Darovasertib in Combination with Crizotinib in 1L HLA*A2-Negative Metastatic Uveal Melanoma

  • IDEAYA Biosciences Unveils OptimUM-02 Data: Darovasertib/Crizotinib Doubles PFS in Uveal Melanoma

  • IDEAYA Biosciences, Inc. (IDYA) Discusses Topline Results from OptimUM-02 Trial Evaluating Darovasertib and Crizotinib in HLA-A2-Negative Metastatic Uveal Melanoma Transcript

  • IDEAYA Eye Cancer Trial Data Beats Standard Therapy, Stock Soars

  • Ideaya Biosciences Stock Jumps 15% on Eye Cancer Therapy Trial Results

  • IDEAYA Biosciences and Servier Announce Positive Topline Results from Phase 2/3 Registrational Trial (OptimUM-02) of Darovasertib in Combination with Crizotinib in First-line HLA-A*02:01-Negative Metastatic Uveal Melanoma