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Table 5 Ongoing clinical trials of immune-checkpoint inhibitors combined with non-cytotoxic agents

From: Immunotherapy in small-cell lung cancer: from molecular promises to clinical challenges

Clinical trial ID

Phase

Setting

Regimen

Endpoint

NCT03041311

II

1st line

CE plus atezolizumab +/− Trilaciclib

OS

AEs

NCT02922764

I

2nd line (solid tumors)

RGX-104 +/− Nivolumab

MTD

ORR

PFS

NCT02712905

I/II

≥ 2nd line (solid tumors)

INCB059872 plus Nivolumab (part 3)

AEs

NCT03126110

I/II

≥ 2nd line

INCAGN01876 plus nivolumab/ipilimumab/nivo+ipi

AEs

ORR

NCT03241173

I/II

≥ 2nd line

INCAGN01949 plus nivolumab/ipilimumab/nivo+ipi

AEs

ORR

NCT03026166

I/II

≥ 2nd line

Rova-T plus Nivolumab +/− ipilimumab

DLT

NCT03085849

I

2nd line

SGI-110 followed by Durvalumab plus Tremelimumab

MTD

NCT02734004 (MEDIOLA)

I/II

2nd line

Durvalumab plus olaparib

DCR

ORR

AEs

NCT02554812

Ib/II

≥ 2nd line

Avelumab plus utomilumab

DLT

OR

  1. PFS Progression Free Survival, ORR Overall Response Rate, RGX-104 LXR inhibitor, MTD Maximum Tolerated Dose, INCB059872 LSD1 inhibitor, AEs Adverse Events, Rova-T Rovalpituzumab Tesirine, DLT Dose limiting toxicities, INCAGN01876 anti-GITR antibody, INCAGN01949 anti-OX40 antibody, SGI-110 DNMT inhibitor, Trilaciclib CDK4/6 inhibitor, Utomilumab anti-CD137 antibody