PUBLISHER: Mordor Intelligence | PRODUCT CODE: 1851281
PUBLISHER: Mordor Intelligence | PRODUCT CODE: 1851281
The global drug discovery market size stands at USD 106.70 billion in 2025 and is forecast to reach USD 146.80 billion by 2030, expanding at a 6.59% CAGR.

Growth is propelled by rising chronic disease prevalence, sustained R&D spending, and the accelerating adoption of artificial intelligence across discovery workflows. Large pharmaceutical companies are directing resources toward late-stage assets, while biotechnology firms leverage agile operating models to advance novel modalities. Artificial intelligence shortens candidate identification from years to months and reduces pre-clinical costs, encouraging wider participation from mid-tier players. Precision medicine is steering investment toward targeted therapies and rare-disease programs, and supportive regulatory initiatives are refining expedited pathways for high-unmet-need indications.
Chronic and rare conditions are redefining program priorities, with oncology alone attracting 41% of active projects due to high unmet need and commercial potential. Neuroscience pipelines are also expanding as companies pursue therapies for Alzheimer's disease, essential tremor, and other debilitating disorders. The trend extends to orphan indications: 88% of novel cell and gene therapies approved in 2024 carried Orphan Drug designations, underscoring a pivot toward smaller, genetically defined populations. Investment in rare disease research drives sophisticated biomarker strategies, improving target validation and de-risking early development. These dynamics collectively lift demand for advanced discovery platforms and attract specialized capital, bolstering long-run growth of the drug discovery market.
Global R&D returns rose to 5.9% in 2024 after the launch of 29 blockbuster drugs, prompting companies to channel resources into late-stage assets with clearer paths to market. Venture funding in life sciences increased 10% year-over-year in Q3 2024, reflecting renewed confidence despite macroeconomic uncertainty. Partnerships surged, with 105 AI-centric discovery deals registered in 2025 as firms sought computational expertise to boost productivity. Capital is becoming more selective, favoring programs with strong mechanistic rationale, regulatory clarity, and differentiated value propositions. Sustained inflows underpin a robust innovation cycle, supporting the expansion of the drug discovery market.
Average outlay per successful asset climbed to USD 2.23 billion, a burden acutely felt by small and mid-cap innovators. Traditional 10-15-year pathways strain capital and delay patient access, especially for complex modalities requiring bespoke manufacturing. Opportunity costs rise as funds remain tied up in protracted programs. Companies counter these pressures by embracing AI-enabled platforms that cut pre-clinical discovery by four years and slash experimental iterations. Risk-sharing collaborations distribute costs, while contract research organizations provide modular capacity, yet financing constraints persist in regions lacking deep capital markets, tempering overall drug discovery market growth.
Other drivers and restraints analyzed in the detailed report include:
For complete list of drivers and restraints, kindly check the Table Of Contents.
Cell and gene therapy candidates expand at a 12.8% CAGR, eclipsing overall drug discovery market growth as curative potential shifts investment priorities. The pipeline of 4,418 advanced therapies reflects surging developer interest, while eight U.S. approvals in 2024 validate regulatory momentum. Small molecules still command 56% of drug discovery market size due to predictable chemistry and established manufacturing, yet growth is decelerating relative to biologics. RNA therapeutics illustrate modality convergence, bridging small-molecule versatility and biologic specificity with projected USD 30 billion sales by 2030. Developers increasingly select modalities based on molecular pathology rather than legacy capability, a strategic realignment reinforcing the dynamism of the drug discovery market.
Adoption of vector engineering and allogeneic cell platforms is improving scalability and lowering cost of goods, enabling wider commercial viability for gene therapies. Meanwhile, peptide and oligonucleotide platforms offer rapid synthesis and favorable toxicity profiles for intracellular targets historically deemed undruggable. Collectively, these shifts diversify the drug discovery market and recalibrate competitive strategies toward platform versatility and modality-agnostic pipelines.
AI-driven CADD grows at a 13.2% CAGR, underpinned by transformer models capable of generating novel chemical entities with optimized ADMET properties. Predictive algorithms evaluate millions of variants in silico, reducing reliance on brute-force screening and trimming cycles in medicinal chemistry. In contrast, high-throughput screening retains the largest share at 32% of the drug discovery market size by leveraging massive compound libraries and established robotics. Integration, not substitution, is the prevailing trend: teams use AI to triage libraries, then deploy HTS on refined subsets, combining computational insight with empirical validation to maximize hit quality.
Pharmacogenomics gains traction by linking genetic variants to drug response, enhancing trial design and post-marketing safety. DNA-encoded libraries offer combinatorial reach while enabling affinity-based selection, complementing AI chemistries. Nanotechnology introduces carrier systems that improve solubility and tissue penetration, broadening target space. Companies that orchestrate these technologies through unified data environments gain speed, accuracy, and lower attrition, thereby enlarging the drug discovery market share of integrated platforms.
The Drug Discovery Market Report is Segmented by Drug Type (Small Molecule, Biologic, and More), Technology (High Throughput Screening, Pharmacogenomics, and More), Process Workflow (Target Identification, Target Validation, and More), Therapeutic Area (Oncology, and More), End User (Pharmaceutical Companies, and More), and Geography (North America, Europe, and More). The Market Forecasts are Provided in Terms of Value (USD).
North America led with 35% of the drug discovery market size in 2024, supported by deep research infrastructure, abundant capital, and seven FDA approvals for advanced therapies in the same year. Venture funding resilience and policy frameworks such as the Rare Disease Innovation Hub sustain momentum. However, average per-drug costs rising to USD 2.23 billion challenge smaller enterprises, spurring adoption of AI-enabled efficiency tools and encouraging cross-border outsourcing of selected functions.
Asia-Pacific is the fastest-growing region, poised for a 10.8% CAGR through 2030. Governments in China, South Korea, and Japan promote AI-rich innovation clusters, streamline trial regulations, and subsidize infrastructure. China alone contributes 23% of global pipeline candidates, reflecting the region's mounting scientific capacity and large patient pools. Antibody-drug conjugate research flourishes, and clinical trial outsourcing benefits from cost-effective operations, reinforcing the region's contribution to the expanding drug discovery market.
Europe maintains a robust scientific base, leveraging Horizon Europe funding mechanisms and pan-EU initiatives aiming to harmonize regulatory review. Focus areas include rare diseases and advanced therapies, with academic-industry consortia accelerating translation. The Middle East & Africa build targeted capabilities in diseases of regional prevalence, supported by sovereign-wealth investment in life-science parks. South America emphasizes natural-product discovery, benefiting from its biodiversity and the NIH's 500,000-sample natural-product library. Cross-regional collaboration intensifies, enabling access to diverse expertise, reducing single-market risk, and collectively enlarging the drug discovery market.