PARP Inhibitors Clinical Trial Pipeline Accelerates As 25+ Pharma Companies Rigorously Develop Drugs For Market Entry Delveinsight
| Drugs | Company | Phase | Indication | RoA |
| Saruparib | AstraZeneca | III | Breast cancer; Prostate cancer | Oral |
| NMS-293 | Nerviano Medical Sciences | II | Astrocytoma; Glioblastoma | Oral |
| SRP-1020 | SciBrunch Therapeutics | I/II | Solid tumors | Oral |
| IDX-1197 | Idience Co., Ltd. | I/II | Solid tumors | Oral |
| GS-0201 | Gilead Sciences | I | Advanced Solid Tumors | Oral |
| MOMA-989 | MOMA Therapeutics | Preclinical | Cancer | Oral |
As per Stuti Mahajan, consulting manager at DelveInsight, PARP inhibitors have firmly established themselves in oncology by targeting DNA repair defects, especially in BRCA-mutated cancers, with momentum fueled by the growing shift toward precision, biomarker-driven care. As their use expands into earlier lines and combination therapies, adoption continues to rise, though high costs and resistance are likely to keep long-term growth measured.
Recent Developments in the PARP Inhibitor Treatment Space
- In April 2026, Acerand Therapeutics announced updated results from its first-in-human Phase I/II study ACE-106-001 (NCT06380660) evaluating ACE-106 (ACE-86225106) in patients with advanced solid tumors. In February 2026, Allarity Therapeutics, Inc. announced that the first patients had been dosed with stenoparib and temozolomide in the VA-funded investigator-initiated Phase II trial for the treatment of relapsed small cell lung cancer (SCLC). In October 2025, Synnovation Therapeutics announced clinical collaboration with DualityBio to evaluate the combination of SNV1521, a next-generation, CNS-penetrant PARP1-selective inhibitor with Duality's HER3 ADC, DB-1310. In May 2025, Acerand Therapeutics announced preliminary clinical data of its self-developed novel and selective PARP1 inhibitor, ACE-86225106. In January 2025, MOMA Therapeutics announced the in-licensing of a next-generation selective PARP1 (poly ADP-ribose polymerase) inhibitor, now known as MOMA-989. In March 2024, Synnovation Therapeutics announced that the first patient has been dosed in a Phase I trial evaluating SNV1521 in patients with solid tumors. In January 2024, IMPACT Therapeutics announced that the first patient in the United States has been treated with EIK1003 (formerly IMP1734), a PARP1 selective inhibitor which was discovered by IMPACT Therapeutics and undergoing global clinical development in collaboration with Eikon Therapeutics.
Scope of the PARP Inhibitors Pipeline Report
- Coverage: Global PARP Inhibitors Therapeutic Assessment By Product Type: Mono, Combination, Mono/Combination PARP Inhibitors Therapeutic Assessment By Clinical Stages: Discovery, Pre-clinical, Phase I, Phase II, Phase III PARP Inhibitors Therapeutics Assessment By Route of Administration: Infusion, Intradermal, Intramuscular, Intranasal, Intravaginal, Oral, Parenteral, Subcutaneous, Topical PARP Inhibitors Therapeutics Assessment By Molecule Type: Vaccines, Monoclonal antibody, Peptides, Polymer, Small molecule Key PARP Inhibitors Companies: AstraZeneca, Nerviano Medical Sciences, SciBrunch Therapeutics, Idience Co., Ltd., MOMA Therapeutics, Allarity Therapeutics, Synnovation Therapeutics, 1cBio, Eikon Therapeutics, Acerand Therapeutics, Gilead Sciences, AtlasMedx, Tasly Pharmaceutical Group and others Key Pipeline PARP Inhibitors: Saruparib, NMS-293, SRP-1020, IDX-1197, MOMA-989, Stenoparib, SNV1521, OC-3, EIK1003, ACE-86225106, GS-0201, AMXI-5001, TSL 1502, and others
Table of Contents
| 1. | PARP Inhibitors Pipeline Report Introduction |
| 2. | PARP Inhibitors Pipeline Report Executive Summary |
| 3. | PARP Inhibitors Pipeline: Overview |
| 4. | Analytical Perspective In-depth Commercial Assessment |
| 5. | PARP Inhibitors Clinical Trial Therapeutics |
| 6. | PARP Inhibitors Pipeline: Late-Stage Products (Pre-registration) |
| 7. | PARP Inhibitors Pipeline: Late-Stage Products (Phase III) |
| 8. | PARP Inhibitors Pipeline: Mid-Stage Products (Phase II) |
| 9. | PARP Inhibitors Pipeline: Early-Stage Products (Phase I) |
| 10. | PARP Inhibitors Pipeline Therapeutics Assessment |
| 11. | Inactive Products in the PARP Inhibitors Pipeline |
| 12. | Company-University Collaborations (Licensing/Partnering) Analysis |
| 13. | Key Companies |
| 14. | Key Products in the PARP Inhibitors Pipeline |
| 15. | Unmet Needs |
| 16. | Market Drivers and Barriers |
| 17. | Future Perspectives and Conclusion |
| 18. | Analyst Views |
| 19. | Appendix |
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