Drugs / IMP1734
last change Jul 2026 re-read 3 minutes ago

IMP1734

targets PARP1 via inhibition

Developed for
neoplasm
Investigated by
Eikon Therapeutics · Impact Therapeutics, Inc.

Trials 1

2024202520262027
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 1/2 NCT06253130 Dec 2023 → Jun 2027 expected neoplasm Eikon Therapeutics Recruiting No outcome recorded

News releases announcing trial results or a regulatory action · 5

DateIssuerRelease
2026-07-20 Impact Therapeutics, Inc. Results ESMO 2026 | 塞纳帕利及PARP1选择性抑制剂(IMP1734、IMP1707)的研究结果入选ESMO impacttherapeutics.com ↗
我们很高兴塞纳帕利及我们的两款新型选择性 PARP1 抑制剂 IMP1734 和 IMP1707 的最新临床数据已被接收在 2026 年 ESMO 年会上进行展示。
2026-06-01 Impact Therapeutics, Inc. Results ASCO 2026 | 英派药业以壁报形式公布 PARP1 选择性抑制剂 IMP1734(EIK1003)单药及联合紫杉醇最新临床数据 impacttherapeutics.com ↗
在49名可评估晚期实体瘤患者中,客观缓解率(ORR)为14.3%,7例均为部分缓解(PR)。
2025-05-30 Impact Therapeutics, Inc. Results 英派药业宣布PARP1选择性抑制剂的数据及临床进展将于2025年ASCO年会上公布 impacttherapeutics.com ↗
PARP1选择性抑制剂IMP1734(EIK1003)首次安全性与疗效数据公布
2023-09-25 Impact Therapeutics, Inc. Regulatory 英派药业宣布PARP1选择性抑制剂(IMP1734)获得美国FDA临床试验许可 impacttherapeutics.com ↗
英派药业宣布,由其自主研究发现,与Eikon Therapeutics合作开发的PARP1选择性抑制剂(IMP1734)已获得美国食品药品监督管理局 (FDA)的临床试验许可,并将于2023年第四季度开展临床I期研究。
2023-09-11 Eikon Therapeutics Regulatory Eikon Therapeutics Announces Business Update Highlighting Pipeline and Clinical Development Progress eikontx.com ↗
Separately, the FDA has cleared IMP1734, a highly selective PARP1 inhibitor developed in partnership with Impact Therapeutics, for Phase 1 study initiation, which will also begin in the fourth quarter.

Evidence & citations 4 cited values

Every value below carries the sentence it was read from. 1 source stands behind the page.

FieldValueCited text
Known as IMP1734 ClinicalTrials.gov intervention name — accepted as the source's own label NCT06253130 ↗
Action Inhibit “PARP1 selective inhibitor” NCT06253130 ↗
Route Oral “IMP1734 monotherapy; oral tablet(s) daily” NCT06253130 ↗
Target PARP1 “PARP1 selective inhibitor” NCT06253130 ↗