Chronic Myeloid Leukemia Clinical Trial Pipeline Appears Robust With 25+ Key Pharma Companies Actively Working In The Domain Delveinsight
| Drugs | Company | Phase | MoA | RoA |
| RS 5614 | Renascience | III | Plasminogen activator inhibitor-1 inhibitor | Oral |
| TERN-701 | MSD | I/II | BCR-ABL tyrosine kinase inhibitor | Oral |
| MGD024 | MacroGenics/Gilead Sciences | I | Anti-CD123 × CD3 | Intravenous |
| ELVN-001 | Enliven Therapeutics | I | Bcr-Abl tyrosine kinase inhibitor | Oral |
| KF 1601 | ImmunoForge | I | Bcr-Abl tyrosine kinase | Oral |
As Stuti Mahajan, consulting manager at DelveInsight, chronic myeloid leukemia is driven by the BCR::ABL1 fusion, with tyrosine kinase inhibitors (TKIs) transforming it into a largely manageable long-term disease. The market is evolving from established TKI therapies toward newer, more selective agents and treatment strategies aimed at addressing resistance, intolerance, deeper molecular responses, and treatment-free remission, supporting continued innovation despite a mature treatment landscape.
Recent Developments in Chronic Myeloid Leukemia Treatment Space
- In June 2026, Enliven Therapeutics, Inc. presented updated positive data from the Phase I ENABLE clinical trial evaluating ELVN-001 in patients with previously treated chronic myeloid leukemia (CML). In July 2026, Mendus AB announced successful recruitment of the first stage of the VITAL-CML trial, comprising the first 8 patients. This marks an important milestone in the development of the company's lead product vididencel in chronic myeloid leukemia (CML). In May 2026, Merck announced the successful completion of the acquisition of Terns Pharmaceuticals, Inc. The addition of TERN-701, a novel investigational oral allosteric BCR::ABL1 tyrosine kinase inhibitor, further diversifies Merck's oncology pipeline. In April 2026, Terns Pharmaceuticals, Inc. announced that the US Food and Drug Administration (FDA) granted Breakthrough Therapy Designation to TERN-701, a novel, oral allosteric BCR::ABL1 inhibitor, for the treatment of adult patients with Ph+ CML in the chronic phase without the T315I mutation previously treated with two or more TKIs. In April 2026, Mendus AB announced that the first patient has been enrolled in the VITAL-CML trial, which evaluates Mendus' lead product vididencel in chronic myeloid leukemia (CML). In January 2025, ImmunoForge announced that it has received approval for the Phase I clinical trial IND for KF1601, a treatment for Chronic Myelogenous Leukemia (CML), from the Korea Ministry of Food and Drug Safety.
Scope of the Chronic Myeloid Leukemia Pipeline Report
- Coverage: Global Chronic Myeloid Leukemia Therapeutic Assessment By Product Type: Mono, Combination, Mono/Combination Chronic Myeloid Leukemia Therapeutic Assessment By Clinical Stages: Discovery, Pre-clinical, Phase I, Phase II, Phase III Chronic Myeloid Leukemia Therapeutics Assessment By Route of Administration: Intra-articular, Intraocular, Intrathecal, Intravenous, Ophthalmic, Oral, Parenteral, Subcutaneous, Topical, Transdermal Chronic Myeloid Leukemia Therapeutics Assessment By Molecule Type: Oligonucleotide, Peptide, Small molecule Chronic Myeloid Leukemia Therapeutics Assessment By Mechanism of Action: Plasminogen activator inhibitor-1 inhibitor, Bcr-Abl tyrosine kinase inhibitor, Anti-CD123 × CD3, and others Key Chronic Myeloid Leukemia Companies: Merck & Co., Inc., Enliven Therapeutics, ImmunoForge, Renascience, MacroGenics, Gilead Sciences, Mendus AB, Shenzhen TargetRx Co., Ltd., Chia Tai Tianqing Pharmaceutical Group, Crossbow Therapeutics, Inc., Shenzhen Zhenxing Medical Technology and others. Key Chronic Myeloid Leukemia Pipeline Therapies: TERN-701, ELVN-001, KF 1601, RS 5614, MGD024, Vididencel, TGRX-678, TQB3911, CBX-250, CUDC 201 and others.
Table of Contents
| 1. | Chronic Myeloid Leukemia Pipeline Report Introduction |
| 2. | Chronic Myeloid Leukemia Pipeline Report Executive Summary |
| 3. | Chronic Myeloid Leukemia Pipeline: Overview |
| 4. | Analytical Perspective In-depth Commercial Assessment |
| 5. | Chronic Myeloid Leukemia Clinical Trial Therapeutics |
| 6. | Chronic Myeloid Leukemia Pipeline: Late-Stage Products (Pre-registration) |
| 7. | Chronic Myeloid Leukemia Pipeline: Late-Stage Products (Phase III) |
| 8. | Chronic Myeloid Leukemia Pipeline: Mid-Stage Products (Phase II) |
| 9. | Chronic Myeloid Leukemia Pipeline: Early-Stage Products (Phase I) |
| 10. | Chronic Myeloid Leukemia Pipeline Therapeutics Assessment |
| 11. | Inactive Products in the Chronic Myeloid Leukemia Pipeline |
| 12. | Company-University Collaborations (Licensing/Partnering) Analysis |
| 13. | Key Companies |
| 14. | Key Products in the Chronic Myeloid Leukemia Pipeline |
| 15. | Unmet Needs |
| 16. | Market Drivers and Barriers |
| 17. | Future Perspectives and Conclusion |
| 18. | Analyst Views |
| 19. | Appendix |
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