Clinical development failure or delay
The pipeline is still in development, and setbacks in Phase 1/3 trials could postpone or eliminate future revenue.
- Scope
- Varegacestat, IM-1021, IM-3050 and preclinical ADCs
- Materiality
- high
Immunome Inc. is a U.S.-based biotechnology company developing targeted oncology therapies, with a pipeline spanning clinical and preclinical assets. Its lead focus is varegacestat for desmoid tumors, alongside antibody-drug conjugate and radioligand programs aimed at cancer indications with high unmet need.
−3 193,3 %
−3 060,0 %
−23,2 %
14.69
14.69
| % | |
|---|---|
| Lead clinical oncology asset | 0% Varegacestat is the company's most advanced program, targeting desmoid tumors with planned NDA submission. |
| Antibody-drug conjugates | 0% ADC programs include IM-1021 and multiple preclinical solid tumor candidates built on the company's target and payload platform. |
| Radioligand therapy | 0% IM-3050 is a FAP-targeted radioligand therapy intended for oncology use after IND clearance. |
| Collaboration revenue | 100% Historical revenue came from a collaboration and option agreement with AbbVie, which has now terminated. |
Immunome does not yet sell approved products commercially; its current 'customers' are primarily regulators, clinical...
Specialized centers that would prescribe varegacestat if approved, because desmoid tumors are a niche oncology indication.
Sites participating in trials and, later, using ADC or radioligand therapies for hematologic and solid tumors.
Pharma or biotech partners that may collaborate on ex-U.S. commercialization or development.
Organizations that will influence reimbursement and access for any approved oncology products.
Immunome is headquartered in the United States and expects to commercialize varegacestat first through a U.S...
The company is prioritizing late-stage development and regulatory preparation for varegacestat while continuing to...
This is the nearest-term value driver and the first potential commercial product.
These programs diversify the pipeline beyond the lead asset and validate the platform.
A wider pipeline increases the chance of future clinical and partnering success.
Immunome remains a development-stage biopharma company with no approved product revenue, so execution risk is...
The pipeline is still in development, and setbacks in Phase 1/3 trials could postpone or eliminate future revenue.
The company has not yet obtained NDA/BLA approval, so commercialization depends on FDA and other regulators.
R&D and launch preparation require substantial capital before product revenue begins.
Larger pharma and biotech peers may reach market first or offer superior efficacy/safety.
Clinical and launch timelines depend on external manufacturing and diagnostic supply chains.
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: 28/04/2026