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AZD5305
Also Known As:
5-(4-((7-ethyl-6-oxo-5,6-dihydro-1,5-naphthyridin-3-yl)methyl)piperazin-1-yl)- N-methylpyridine-2-carboxamide
Networked:
4
relevant articles (
1
outcomes,
1
trials/studies)
Relationship Network
Bio-Agent Context: Research Results
Heterocyclic Compounds: 198
1-Ring Heterocyclic Compounds
Piperazines: 26
AZD5305: 4
Fused-Ring Heterocyclic Compounds
2-Ring Heterocyclic Compounds
Naphthyridines: 2
AZD5305: 4
Related Diseases
1.
Neoplasms (Cancer)
01/01/2023 - "
Addition of AZD5305 sensitized very low B7-H4-expressing tumors to AZD8205 treatment, independent of HRD status and in models representing clinically relevant mechanisms of PARPi resistance.
"
01/01/2023 - "
In BRCA-mutated OC-PDXs, AZD5305 achieved greater tumor regressions and longer duration of response as well as a superior impairment of visceral metastasis and improved survival benefit compared with the first-generation dual PARP1/2 inhibitors.
"
01/01/2023 - "
Combination efficacy was greater against tumors that did not respond well to platinum, even at a dose at which AZD5305 monotherapy was ineffective.
"
11/01/2022 - "
Animal models treated with AZD5305 at doses ≥0.1 mg/kg once daily achieved greater depth of tumor regression compared to olaparib 100 mg/kg once daily, and longer duration of response.
"
2.
Neoplasm Metastasis (Metastasis)
01/01/2023 - "
In BRCA-mutated OC-PDXs, AZD5305 achieved greater tumor regressions and longer duration of response as well as a superior impairment of visceral metastasis and improved survival benefit compared with the first-generation dual PARP1/2 inhibitors.
"
01/01/2023 - "
AZD5305 alone or in combination with platinum delayed visceral metastasis, ultimately extending the lifespan of OC-PDX-bearing mice.
"
01/01/2023 - "
The PARP1 Inhibitor AZD5305 Impairs Ovarian Adenocarcinoma Progression and Visceral Metastases in Patient-derived Xenografts Alone and in Combination with Carboplatin.
"
3.
Prostatic Neoplasms (Prostate Cancer)
01/01/2022 - "
Findings from the phase I/IIa trial of AZD5305, a next-generation, highly selective PARP1 inhibitor, indicate that the drug is better tolerated in patients with ovarian, HER2-negative breast, pancreatic, and prostate cancers with BRCA1/2, PALB2, and RAD51C mutations compared with first-generation PARP inhibitors.
"
4.
DNA Repair-Deficiency Disorders (Chromosome Instability Syndromes)
11/01/2022 - "
AZD5305 potently and selectively inhibits PARP1 resulting in excellent antiproliferative activity and unprecedented selectivity for DNA repair deficient versus proficient cells.
"
5.
Ovarian Neoplasms (Ovarian Cancer)
01/01/2023 - "
We investigated ovarian cancer patient-derived xenografts (OC-PDXs) to assess whether malignant progression could be impaired by a novel inhibitor selective for PARP1 (AZD5305) and to assess the potential of its combination with carboplatin (CPT), the standard-of-care for patients with ovarian cancer.
"
Related Drugs and Biologics
1.
Poly(ADP-ribose) Polymerase Inhibitors
2.
Carboplatin (JM8)
3.
Platinum
4.
olaparib
5.
2- cyclohexylidenhydrazo- 4- phenyl- thiazole