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Acelarin

Alternative Names: acelarin, nuc-1031, nuc1031, nuc 1031
Latest Update: 2024-04-19
Latest Update Note: PubMed Publication

Product Description

NUC-1031 (Acelarin), a phosphoramidate transformation of gemcitabine, was the first anti-cancer ProTide to enter the clinic. We find it displays important in vitro cytotoxicity differences to gemcitabine, and a genome-wide CRISPR/Cas9 genetic screening approach identified only the pyrimidine metabolism pathway as modifying cancer cell sensitivity to NUC-1031. (Sourced from: https://pubmed.ncbi.nlm.nih.gov/31113993/)

Mechanisms of Action: No Mechanism

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Intravenous

FDA Designation: Fast Track - Biliary Tract Cancer *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Nucana
Company Location: EDINBURGH X0 EH12 9DT
Company CEO:
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Acelarin

Countries in Clinic:

Active Clinical Trial Count:

Highest Development Phases

Phase 3: Biliary Tract Cancer|Pancreatic Cancer|Adenocarcinoma|Acinar Cell Carcinoma|Gallbladder Cancer

Phase 2: Fallopian Tube Cancer|Ovarian Cancer

Phase 1: Biliary Tract Cancer|Liver Cancer|Cholangiocarcinoma|Gallbladder Cancer|Ovarian Cancer

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

2019-001025-28

P3

Unknown status

Adenocarcinoma|Gallbladder Cancer|Biliary Tract Cancer

2023-06-06

NuTide:121

P3

Terminated

Biliary Tract Cancer

2022-03-02

ACELARATE

P3

Suspended

Pancreatic Cancer|Acinar Cell Carcinoma

2020-09-01

PRO-105

P2

Terminated

Ovarian Cancer

2019-12-31

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