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. 2021 May 10;14:17562848211014818. doi: 10.1177/17562848211014818

Table 3.

Ongoing clinical trials investigating novel targeting agents.

PARP inhibitors Eligibility based on targeted genetic mutation Combination Study phase Treatment setting Sponsor Clinicaltrials.gov identifier Estimated study completion time
Olaparib Germline BRCA1/2 None II Any AstraZeneca NCT01078662 31 December 2021
Genetic aberrations associated with HRD,* must be germline BRCA1/2 negative None II Second line AstraZeneca NCT02677038 30 November 2022
No specific genetic targets Cediranib (VEGF inhibitor) II Second line National Cancer Institute NCT02498613 31 December 2021
Germline BRCA1/2 Pembrolizumab II Second line National Cancer Institute NCT04548752 31 March 2025
No specific genetic targets None (cobimetinib as parallel arm) I Any OHSU Knight Cancer Institute NCT04005690 1 February 2025
No specific genetic targets, ARID1A/ATM loss subgroup AZD6738 (ATR kinase inhibitor) II Second line or more AstraZeneca NCT03682289 19 March 2023
No specific genetic targets AZD5153 (BET/BRD4 bromodomain inhibitor) I Second line or more AstraZeneca NCT03205176 30 March 2021
No specific genetic targets Multi-agents low dose chemotherapy followed by maintenance pembrolizumab II First line Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins NCT04753879 April 2025
Rucaparib Germline or somatic BRCA1/2 or PALB2 None II Maintenance Abramson Cancer Center, UPenn NCT03140670 1 June 2022
No specific genetic targets Liposomal irinotecan, 5-fluorouracil and leucovorin I/II Any Academic and Community Cancer Research United NCT03337087 1 July 2022
Germline or somatic BRCA 1/2, PALB2, RAD51C, RAD51D, BARD1, FANCA, NBN, RAD51, or RAD51B None II Second line or more Clovis Oncology, Inc. NCT04171700 May 2022
Niraparib No specific genetic targets Ipilimumab or nivolumab I/II Second line Upenn NCT03404960 December 2021
No specific genetic targets None II Any University of Kansas Medical Center NCT03553004 1 February 2025
Germline or somatic BRCA1/2, PALB2, CHEK2 or ATM None II Second line or more Dana-Farber Cancer Institute NCT03601923 28 February 2025
No specific genetic targets Dostarlimab plus radiation II Any Massachusetts General Hospital NCT04409002 1 October 2026
Germline or somatic BRCA1/2, PALB2, BARD1, RAD51c, RAD51d Dostarlimab II Second and third line Mayo Clinic NCT04493060 1 December 2022
Germline or somatic BRCA1/2, ATM, ATR, BAP1, BRIP1, CHEK2, FANCA, PALB2, RAD51 Anlotinib I Second line Beijing Cancer Hospital NCT04764084 28 February 2023
Germline or somatic BRCA1/2 TSR-042 Ib Second line or more University of Washington NCT04673448 30 March 2026
Talazoparib Genes involved in DDR,** deleterious mutations confer sensitivity to PARP inhibitors (germline or somatic)+ None II Any National Cancer Institute NCT04550494 1 December 2023
Veliparib No specific genetic targets FOLFIRI or mFOLFIRI II Second line National Cancer Institute NCT02890355 1 May 2019 (completed)
Personal or family history of mutation in BRCA1/2, PALBB2, or one of the FANC genes mFOLFOX6 I/II Any Georgetown University NCT01489865 31 December 2020
Germline or somatic BRCA1/2 or PALB2 Cisplatin and gemcitabine II Any National Cancer Institute NCT01585805 1 December 2021
No specific genetic targets Irinotecan hydrochloride I Any National Cancer Institute NCT00576654 30 June 2021
*

Homologous recombination deficiency.

**

DNA damage response.

+

Deleterious BRCA1 or BRCA2 mutations, loss of function mutations in FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ, FANCL, FANCM, FANCN. A known functional mutation in ATM, BACH1 (BRIP1), BARD1, CDK12, CHK1, CHK2, IDH1, IDH2, MRE11A, NBN, PALB2, RAD50, RAD51, RAD51B, RAD51C, RAD51D, RAD54L.

Last accessed date of clinicaltrials.gov: 8 March 2021.