MedPath

Immuneering

🇺🇸United States
Ownership
-
Employees
68
Market Cap
$33.5M
Website
Introduction

Immuneering Corp. operates as a clinical-stage oncology company, which engages in developing medicines for cancer patients. Its pipeline of drug candidates focuses on treating aspects of disease that have eluded conventional approaches, including cancer cachexia and metastasis. The company was founded by Robert J. Carpenter and Benjamin J. Zeskind in 2008 and is headquartered in Cambridge, MA.

newsfilecorp.com
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Immunotherapy Clinical Trials - A New Approach to Treating Cancer

Immunotherapy clinical trials show promise for long-term survival in various cancers, with Aethlon Medical's Hemopurifier® designed to improve response rates to anti-PD-1 therapies by removing tumor-derived extracellular vesicles. Positive initial data from Immuneering Corporation's Phase 2a trial of IMM-1-104 in pancreatic cancer and Iovance Biotherapeutics' lifileucel in advanced melanoma further support the potential of immunotherapy.
investorideas.com
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Immunotherapy Clinical Trial News - Stocks to Watch

Aethlon Medical's Hemopurifier®, an immunotherapeutic device for cancer, gains ethics approval in India for a trial in solid tumor patients resistant to anti-PD-1 therapy. The trial aims to assess safety and feasibility, with potential to improve response rates to anti-PD-1 antibodies by removing tumor-produced extracellular vesicles.
stocktitan.net
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Innovation Driving Cancer's Solid Tumors Market

Solid tumors market projected to reach $375.4B by 2034 with 7.45% CAGR. Aethlon Medical activates Hemopurifier trial at Royal Adelaide Hospital for solid tumor patients resistant to anti-PD-1 therapies. Immuneering reports positive initial data for IMM-1-104 in pancreatic cancer. FDA approves new immunotherapy combinations for endometrial cancer from AstraZeneca, Merck, and GlaxoSmithKline. Roche's trastuzumab deruxtecan receives accelerated approval for HER2-positive solid tumors.
biospace.com
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Immuneering Announces Positive Initial Phase 2a Data for IMM-1-104 in Pancreatic Cancer

Initial Phase 2a trial results for IMM-1-104 combined with gemcitabine/nab-paclitaxel in pancreatic cancer show a 40% response rate and 80% disease control rate among the first five patients. IMM-1-104 is well-tolerated, with further dosing at 320 mg QD approved. Data aligns with preclinical findings, indicating potential for deeper responses than chemotherapy alone.
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