Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
IMO-2055 + erlotinib + bevacizumab is an investigational three-drug combination studied primarily in advanced or metastatic non-small cell lung cancer (NSCLC) patients who have progressed following chemotherapy. IMO-2055 is a synthetic, immunostimulatory oligonucleotide that acts as a Toll-like receptor 9 (TLR9) agonist, activating innate immunity and potentially enhancing tumor-directed immune responses[1][3][5][7]. Erlotinib is a small molecule, reversible tyrosine kinase inhibitor (TKI) targeting the epidermal growth factor receptor (EGFR), used in various cancers including NSCLC. Bevacizumab is a monoclonal antibody against vascular endothelial growth factor A (VEGF-A), inhibiting angiogenesis and thus tumor growth[2][4][6][8]. The reported mechanism for this combination is to synergistically enhance antitumor efficacy by combining immune stimulation (IMO-2055), blockade of EGFR signaling (erlotinib), and suppression of tumor neoangiogenesis (bevacizumab). The triple therapy showed tolerable safety and anecdotal antitumor activity in early-phase clinical trials for heavily pretreated NSCLC patients[1][3][5][7].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on IMO-2055 + erlotinib + bevacizumab.