Drugs / PRT3789

Trials 2

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 11 trial
Phase 1 NCT05639751 May 2023 → Oct 2025 metastatic neoplasm, non-small cell lung carcinoma Prelude Therapeutics Completed No outcome recorded
Phase 21 trial
Phase 2 NCT06682806 Jun 2025 → Jan 2026 esophageal cancer, metastatic malignant neoplasm, non-small cell lung carcinoma Prelude Therapeutics Terminated No outcome recorded Stop: Business

News releases announcing trial results or a regulatory action · 7

DateIssuerRelease
2024-10-24 Prelude Therapeutics Results Prelude Therapeutics Presents New Data from SMARCA Degrader Portfolio at the 36th EORTC-NCI-AACR Symposium preludetx.com ↗
Interim data from ongoing trial of PRT3789 showed additional clinical activity at higher doses in patients with non-small cell lung cancer (NSCLC)
2024-09-13 Prelude Therapeutics Results Prelude Therapeutics’ SMARCA2 Degrader PRT3789 Demonstrated Promising Initial Clinical Activity and Safety Profile in Phase 1 Trial preludetx.com ↗
Overall, of the 26 advanced, heavily pre-treated NSCLC or esophageal patients evaluable for efficacy, 7 had tumor shrinkage.
2024-09-09 Prelude Therapeutics Results Prelude Therapeutics Announces Publication of Abstract for Presentation at the European Society of Medical Oncology (ESMO) Congress 2024 preludetx.com ↗
Although PRT3789 as a first-in-class molecule targeting a novel mechanism is early in its development, we are highly encouraged by the safety profile, target engagement and clinical activity we have seen to date.
2024-04-09 Prelude Therapeutics Results Prelude Highlights Continued Strength of Discovery Engine at 2024 AACR Annual Meeting preludetx.com ↗
Next Generation CDK4/6 Inhibitor, PRT3645, is highly effective in combination with other targeted therapies in preclinical models of breast cancer, CRC and NSCLC
2022-11-14 Prelude Therapeutics Regulatory Prelude Therapeutics Announces Third Quarter 2022 Financial Results and Provides Business Update preludetx.com ↗
We made meaningful advancements in the third quarter and to date in the fourth quarter, including FDA clearance for two new INDs, one for PRT3645, a next generation, brain penetrant CDK4/6 inhibitor and one for PRT3789, a novel, first-in-class selective SMARCA2 degrader.
2022-10-18 Prelude Therapeutics Regulatory Prelude Therapeutics Receives FDA Clearance of IND for PRT3789, a Potent and Selective First-in-Class SMARCA2 Protein Degrader preludetx.com ↗
Clearance of the IND for PRT3789 represents a major milestone for Prelude Therapeutics, as we advance our first-in-class SMARCA2 protein degrader from discovery to the clinic.
2022-03-09 Prelude Therapeutics Results Prelude Therapeutics Provides Clinical Update and Announces Presentation of New Preclinical Data at the Upcoming 2022 AACR Annual Meeting preludetx.com ↗
The abstract highlights new preclinical data demonstrating synergistic benefit when PRT1419 was combined with the Company’s novel and selective SMARCA2 degrader, PRT3789, in SMARCA4 deleted lung cancer models.

Evidence & citations 4 cited values

Every value below carries the sentence it was read from. 2 sources stand behind the page.

FieldValueCited text
Known as PRT3789 ClinicalTrials.gov intervention name — accepted as the source's own label NCT05639751 ↗
1

NCT06682806 ↗

Modality Other / unclassified “PRT 3789, a first-in-class SMARCA2 targeted protein degrader” NCT06682806 ↗
Route Intravenous “PRT3789 will be administered by intravenous infusion” NCT05639751 ↗
Target SMARCA2 “a SMARCA2 degrader” NCT05639751 ↗