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PUBLISHER: Mellalta Meets LLP | PRODUCT CODE: 1517292

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PUBLISHER: Mellalta Meets LLP | PRODUCT CODE: 1517292

CDK2 Inhibitor - Pipeline Analytics 2024

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The 2024 Mellalta Meets report analyzes the CDK2 inhibitor pipeline landscape, highlighting the market opportunities and competitive landscape with over 32 companies developing pipeline drug profiles.

Cyclin-dependent kinase 2 (CDK2) is a pivotal protein kinase that orchestrates cell division and the cell cycle. Dysregulation of CDK2 has been implicated in various cancers, making it an attractive target for therapeutic intervention.

CDK2 inhibitors present a compelling investment opportunity. These inhibitors target critical cell cycle dynamics, offering therapeutic potential across multiple high-burden cancer types such as Breast and Ovarian Cancer.

The CDK2 inhibitor market is highly dynamic and competitive with over 36 products with key players, including Sino Biopharma, Tiziana Life Sciences, Incyclix Bio, Pfizer, Cyclacel Pharmaceuticals, and Blueprint Medicines. These companies are pursuing various indications for CDK2 inhibitors, such as ER+/HER2- breast cancer, non-small cell lung cancer, dedifferentiated liposarcoma, ovarian cancer, unresectable/metastatic hepatocellular carcinoma, and CCNE1-amplified cancers.

With a robust pipeline and promising clinical data, these inhibitors represent a high-reward opportunity in the oncology landscape. Numerous small molecule inhibitors have been identified for their CDK2 inhibitory activity. However, the development of these inhibitors is fraught with challenges, particularly regarding specificity due to the structural similarities among cyclin-dependent kinases (CDKs).

Efforts are ongoing to engineer inhibitors that selectively target CDK2, thereby minimizing off-target effects and enhancing therapeutic efficacy. As research progresses, CDK2 inhibitors are poised to play a transformative role in overcoming CDK4/6 resistance, offering significant benefits for patients and lucrative opportunities for investors with the usage of different CDK2 targeting strategies such as protein-protein interaction, Allosteric, Orthosteric, and indirect inhibition.

The CDK2 Inhibitor - Pipeline Analytics -2024 report published by Mellalta Meets covers the Cell Therapies market opportunity providing Key Competitive Analysis, 32+ Companies and 36 Products with Pipeline Drug Profiles, Clinical Trials, Other Developments (Collaboration Details, Funding, etc.), Licensing and Agreements, Business Agreement, Business Partner as well as Clinical Partner. Reports cover pipeline product analysis by stage of development, competitive landscape by phases, companies, clinical trials by regions, and intervention type. CDK2 Inhibitor-Pipeline Analytics report adds value in terms of describing clinical-stage products for their clinical & regulatory timelines as well as in terms of providing the current market opportunity, drivers, and challenges.

Mellalta's CDK2 Inhibitor Pipeline Report - Key Highlights

The CDK2 inhibitors market is highly competitive, with over 36 inhibitors. The majority are in the early stage, with 38.89% in the Discovery stage, 19.44% in the pre-clinical stage, and 19.44% in Phase 1. Phase 1/2 products make up 16.67% of the total, while Phase 3 and Phase 2 products each represent 2.78%.

Among the key players, Blueprint Medicines and Pfizer stand out with the highest number of assets, totaling three in its portfolio.

Allosteric inhibitors are favored and preferred mechanisms due to their low toxicity profiles.

Cyclins are being directly targeted as a focused approach to avoid toxicity.

Report Coverage:

Indication Prioritization: CDK2 Inhibitor market potential

Business Transactions & Strategies: Key collaborations and deal values

CDK2 Inhibitor Pipeline Development: Product Profiles, Clinical Trials & Results

CDK2 Inhibitor Acquisition Targets

CDK2 Inhibitor Competitive Intelligence

Recent and upcoming events

Table of Content

1. OVERVIEW

2. The CDK2 Inhibitor Target BACKGROUND

  • 2.1. Introduction and Role of CDK2 inhibitors
  • 2.2. Potential Concern with CDK4/6 Inhibitors
  • 2.3. CDK2 Inhibitors: A Highly-Potential Target in Oncology Space
  • 2.4. Clinical Applications of CDK2 Inhibitors
  • 2.5. Overcoming CDK4/6 Resistance: The Strategic Role of CDK2 Inhibitors
  • 2.6. Allosteric Mechanism of CDK2 Inhibitors

3. CDK2 Inhibitor PIPELINE ANALYSIS by Phases

  • 3.1. CDK2 Inhibitor Development - Overview
  • 3.2. Pipeline Products by Stage of Development
  • 3.3. Pipeline Products by Company
  • 3.4. Pipeline Products by Indication and Phases
  • 3.5. CDK2 Inhibitor Monotherapy & Combinations Clinical Trials
  • 3.6. CDK2 Pipeline: Geographic Distribution of Clinical Trials
  • 3.7. CDK2 Inhibitor Clinical & Regulatory Timelines
  • 3.8. Late-Stage Profiles Comparisons At-a-glance

4. CDK2 Inhibitor LICENSING, ACQUISITION, AND COLLABORATION DEALS

  • 4.1. CDK2 Inhibitor Licensing, Acquisition, and Deal values
  • 4.2. CDK2 Inhibitor Licensing by Transaction type and total amount size by Phases

5. CDK2 Inhibitor Pipeline Landscape

  • 5.1. CDK2 Inhibitor Pipeline Drug Profiles- at a glance
    • 5.1.1. Phase III
      • 5.1.1.1. TQB3616 (Sino Biopharma)
        • 5.1.1.1.1. Product Profile & Description
        • 5.1.1.1.2. Clinical Trials
        • 5.1.1.1.3. Collaborations
        • 5.1.1.1.4. Other Developments
    • 5.1.2. Phase II
      • 5.1.2.1. Milciclib (Tiziana Life Sciences)
        • 5.1.2.1.1. Product Profile & Description
        • 5.1.2.1.2. Clinical Trials
        • 5.1.2.1.3. Collaborations
        • 5.1.2.1.4. Other Developments
    • 5.1.3. Phase I/II
      • 5.1.3.1. INX-315 (Incyclix Bio)
        • 5.1.3.1.1. Product Profile & Description
        • 5.1.3.1.2. Clinical Trials
        • 5.1.3.1.3. Collaborations
        • 5.1.3.1.4. Other Developments
      • 5.1.3.2. Fadraciclib (Cyclacel Pharmaceuticals)
        • 5.1.3.2.1. Product Profile & Description
        • 5.1.3.2.2. Clinical Trials
        • 5.1.3.2.3. Collaborations
        • 5.1.3.2.4. Other Developments
      • 5.1.3.3. PF 07104091 (Pfizer)
        • 5.1.3.3.1. Product Profile & Description
        • 5.1.3.3.2. Clinical Trials
        • 5.1.3.3.3. Collaborations
        • 5.1.3.3.4. Other Developments
      • 5.1.3.4. AVZO-021 (Avenzo Therapeutics/Allorion Therapeutics Inc)
        • 5.1.3.4.1. Product Profile & Description
        • 5.1.3.4.2. Clinical Trials
        • 5.1.3.4.3. Collaborations
        • 5.1.3.4.4. Other Developments
      • 5.1.3.5. AZD 8421 (AstraZeneca)
        • 5.1.3.5.1. Product Profile & Description
        • 5.1.3.5.2. Clinical Trials
        • 5.1.3.5.3. Collaborations
        • 5.1.3.5.4. Other Developments
      • 5.1.3.6. BLU 222 (Blueprint Medicines)
        • 5.1.3.6.1. Product Profile & Description
        • 5.1.3.6.2. Clinical Trials
        • 5.1.3.6.3. Collaborations
        • 5.1.3.6.4. Other Developments
    • 5.1.4. Phase I
      • 5.1.4.1. NKT 3447 (NiKang Therapeutics)
        • 5.1.4.1.1. Product Profile & Description
        • 5.1.4.1.2. Clinical Trials
        • 5.1.4.1.3. Collaborations
        • 5.1.4.1.4. Other Developments
      • 5.1.4.2. BG-68501 (BeiGene)
        • 5.1.4.2.1. Product Profile & Description
        • 5.1.4.2.2. Clinical Trials
        • 5.1.4.2.3. Collaborations
        • 5.1.4.2.4. Other Developments
      • 5.1.4.3. TYK 0540 (TYK Medicine)
        • 5.1.4.3.1. Product Profile & Description
        • 5.1.4.3.2. Clinical Trials
        • 5.1.4.3.3. Collaborations
        • 5.1.4.3.4. Other Developments
      • 5.1.4.4. INCB123667 (Incyte)
        • 5.1.4.4.1. Product Profile & Description
        • 5.1.4.4.2. Clinical Trials
        • 5.1.4.4.3. Collaborations
        • 5.1.4.4.4. Other Developments
      • 5.1.4.5. RGT-419B (REGOR THERAPEUTICS)
        • 5.1.4.5.1. Product Profile & Description
        • 5.1.4.5.2. Clinical Trials
        • 5.1.4.5.3. Collaborations
        • 5.1.4.5.4. Other Developments
      • 5.1.4.6. SYH2043 (CSPC Ouyi Pharmaceutical)
        • 5.1.4.6.1. Product Profile & Description
        • 5.1.4.6.2. Clinical Trials
        • 5.1.4.6.3. Collaborations
        • 5.1.4.6.4. Other Developments
      • 5.1.4.7. WXWH0240 (Cisen Pharmaceutical)
        • 5.1.4.7.1. Product Profile & Description
        • 5.1.4.7.2. Clinical Trials
        • 5.1.4.7.3. Collaborations
        • 5.1.4.7.4. Other Developments
    • 5.1.5. Preclinical
      • 5.1.5.1. IAM-C1 (Iambic Therapeutics)
        • 5.1.5.1.1. Product Profile & Description
        • 5.1.5.1.2. Collaborations
        • 5.1.5.1.3. Other Developments
      • 5.1.5.2. AU14-5 (AUCENTRA)
        • 5.1.5.2.1. Product Profile & Description
        • 5.1.5.2.2. Collaborations
        • 5.1.5.2.3. Other Developments
      • 5.1.5.3. CID-078 (Circle Pharma)
        • 5.1.5.3.1. Product Profile & Description
        • 5.1.5.3.2. Collaborations
        • 5.1.5.3.3. Other Developments
      • 5.1.5.4. CC002 (Chupu Chuangzhi (Wuhan) Pharmaceutical Technology)
        • 5.1.5.4.1. Product Profile & Description
        • 5.1.5.4.2. Collaborations
        • 5.1.5.4.3. Other Developments
      • 5.1.5.5. IpY.20 (Concarlo Therapeutics)
        • 5.1.5.5.1. Product Profile & Description
        • 5.1.5.5.2. Collaborations
        • 5.1.5.5.3. Other Developments
      • 5.1.5.6. CED-2368 (Bayer)
        • 5.1.5.6.1. Product Profile & Description
        • 5.1.5.6.2. Collaborations
        • 5.1.5.6.3. Other Developments
      • 5.1.5.7. TY-1210 (TYK Medicines)
        • 5.1.5.7.1. Product Profile & Description
        • 5.1.5.7.2. Collaborations
        • 5.1.5.7.3. Other Developments
    • 5.1.6. Discovery
      • 5.1.6.1. CDK2 and CCNE1 (Kymera Therapeutics)
        • 5.1.6.1.1. Product Profile & Description
        • 5.1.6.1.2. Collaborations
        • 5.1.6.1.3. Other Developments
      • 5.1.6.2. CDK2 targeting therapeutics (Plexium)
        • 5.1.6.2.1. Product Profile & Description
        • 5.1.6.2.2. Collaborations
        • 5.1.6.2.3. Other Developments
      • 5.1.6.3. CDK2 Inhibitor (Bugworks)
        • 5.1.6.3.1. Product Profile & Description
        • 5.1.6.3.2. Collaborations
        • 5.1.6.3.3. Other Developments
      • 5.1.6.4. CDK2 degraders (Monte Rosa Therapeutics)
        • 5.1.6.4.1. Product Profile & Description
        • 5.1.6.4.2. Collaborations & Other Developments
      • 5.1.6.5. BLU-956 (Blueprint Medicines)
        • 5.1.6.5.1. Product Profile & Description
        • 5.1.6.5.2. Collaborations
        • 5.1.6.5.3. Other Developments
      • 5.1.6.6. TPD: CDK2 (Blueprint Medicines)
        • 5.1.6.6.1. Product Profile & Description
        • 5.1.6.6.2. Collaborations
        • 5.1.6.6.3. Other Developments
      • 5.1.6.7. QR-6401 (REGOR THERAPEUTICS)
        • 5.1.6.7.1. Product Profile & Description
        • 5.1.6.7.2. Collaborations
        • 5.1.6.7.3. Other Developments
      • 5.1.6.8. CDK2 inhibitor (Calibr-Skaggs)
        • 5.1.6.8.1. Product Profile & Description
        • 5.1.6.8.2. Collaborations
        • 5.1.6.8.3. Other Developments
      • 5.1.6.9. Cyclin E/CDK2 inhibitor (Circle Pharma)
        • 5.1.6.9.1. Product Profile & Description
        • 5.1.6.9.2. Collaborations
        • 5.1.6.9.3. Other Developments
      • 5.1.6.10. TMX-2172 (Dana-Farber Cancer Institute)
        • 5.1.6.10.1. Product Profile & Description
        • 5.1.6.10.2. Collaborations
        • 5.1.6.10.3. Other Developments
      • 5.1.6.11. CDK2 Inhibitor (Acellera Therapeutics)
        • 5.1.6.11.1. Product Profile & Description
        • 5.1.6.11.2. Collaborations
        • 5.1.6.11.3. Other Developments
      • 5.1.6.12. FP19711 and FP24322 (Fog Pharma)
        • 5.1.6.12.1. Product Profile & Description
        • 5.1.6.12.2. Collaborations
        • 5.1.6.12.3. Other Developments
      • 5.1.6.13. I-125A and I-198 (Pfizer/ Belharra Therapeutics/ Magnet Biomedicine)
        • 5.1.6.13.1. Product Profile & Description
        • 5.1.6.13.2. Collaborations
        • 5.1.6.13.3. Other Developments

6. Allosteric CDK2 Inhibitor Mechanisms- At a glance

7. CDK2 Inhibitor SWOT Analysis

8. Appendix

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