Announcements Trials
Browse Landscape

Phase

Phase 1 5Phase 2 1

Status

Completed 6Withdrawn 1

Sponsor Class

INDUSTRY 5OTHER 1

Study Type

Interventional 6

Sponsor

Cancer Type

Lymphoid 3Other solid neoplasm 1Gynecologic 1Dermatologic 1

Conditions

Neoplasms 2Lymphoma, Non-Hodgkin 2Solid Tumor Cancer 1Ovarian Neoplasms 1Melanoma 1Lymphoma 1

Interventions

Cyclophosphamide 1492Cisplatin 1414Paclitaxel 1317Radiotherapy 1261Carboplatin 1250Gemcitabine 1215Docetaxel 1109Bevacizumab 1030Fluorouracil 894Doxorubicin 792Dexamethasone 748Rituximab 719Capecitabine 716Oxaliplatin 700pembrolizumab 680Etoposide 678Irinotecan 634Filgrastim 621Cytarabine 586Leucovorin 579Nivolumab 558Vincristine 515Prednisone 475Cetuximab 465Bortezomib 459Erlotinib Hydrochloride 456Trastuzumab 447Methotrexate 438Lenalidomide 427Pemetrexed 420

Date Range

30 days90 days1 yearAll

Options

Has results Has announcements

Clinical Trials

6 trials
RecentStart dateEnrollment
Completed × Interventional × Interleukin-18 × Clear all
NCT01768338 2023-02-10

Recombinant Human IL-18 and Ofatumumab After PBSCT for Lymphoma

Indiana University

Phase 1 Completed
9 enrolled
Lymphoid

Lymphoma, Non-Hodgkin

NCT00107718 2017-07-27

Anti-Tumor Activity Of SB-485232 In Patients With Previously Untreated Metastatic Melanoma

GlaxoSmithKline

Phase 2 Completed
64 enrolled
Dermatologic

Melanoma

NCT00500058 2017-07-26

A Phase I, Dose-Escalation Study to Assess the Safety and Biological Activity of Recombinant Human Interleukin-18

GlaxoSmithKline

Phase 1 Completed
24 enrolled
Lymphoid

Lymphoma, Non-Hodgkin, Neoplasms

NCT00659178 2017-07-21

Combination Study Of SB-485232 (Interleukin 18) And Doxil For Advanced Stage Epithelial Ovarian Cancer

GlaxoSmithKline

Phase 1 Completed
15 enrolled
Gynecologic

Ovarian Neoplasms

NCT00085878 2008-10-16

Dose-Escalation Study Of SB-485232 Administered As Daily Subcutaneous Injections In Adults With Solid Tumors

GlaxoSmithKline

Phase 1 Completed
25 enrolled
Other solid neoplasm

Solid Tumor Cancer

NCT00085904 2008-10-13

Dose-Escalating Study Of SB-485232 Administered Intravenously Every 28 Days To Adults With Solid Tumors Or Lymphomas

GlaxoSmithKline

Phase 1 Completed
12 enrolled
Lymphoid

Lymphoma, Neoplasms

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