Clinical-stage biotech developing LAG-3-based immunotherapies for cancer and autoimmune disease; lead asset eftilagimod alpha is in Phase 2/3 for breast cancer and HNSCC.
No capital raise or buyback data
Peer-reviewed papers & conference abstracts via PubMed
Historical delivery and spending consistency — data is limited for recently added companies.
Outcome quality (positive/negative readouts) reflects the science, not execution — shown above but excluded from the score.
These metrics reflect historical operational data only. They are not predictive of future performance, do not constitute investment advice, and should not be used as the basis for any investment decision.
These changes were automatically detected by comparing ClinicalTrials.gov records over time. A slipped date means the trial's expected completion moved later; pulled forward means it moved earlier.
No cash flow data
| Event | Type | Confidence | Impact | Date | Status |
|---|---|---|---|---|---|
| IMP761 Phase I data at EULAR 2026 SAD Phase I results for LAG-3 agonist IMP761 to be presented at EULAR Congress, London; dose-dependent T cell suppression demonstrated | conference presentation | Confirmed | arrow_upwardHigh | 4 June 2026 | Upcoming |
| IMP761 Phase I data at EULAR 2026 SAD/MAD data for first-in-class LAG-3 agonist in autoimmune disease | conference presentation | Confirmed | arrow_upwardHigh | 4 June 2026 | Upcoming |
| IMP761 Phase I MAD portion completionopen_in_new The multiple ascending dose (MAD) portion of the Phase I study is currently ongoing across two dose levels, with completion expected in Q3 2026. [Source: Update on Phase I Study of IMP761 for Autoimmune Diseases, 2026-03-18] | data readout | Expected | arrow_upwardHigh | 30 Sept 2026 | Upcoming |
| IMP761 Phase I MAD completion Multiple ascending dose cohorts ongoing; no safety issues to date; completion guides Phase II dose selection | data readout | Expected | arrow_upwardHigh | 30 Sept 2026 | Upcoming |
| TACTI-003 HNSCC registrational path decision FDA feedback on registrational or single-arm trial pathway for CPS<1 HNSCC | regulatory decision | Speculative | arrow_upwardHigh | 31 Dec 2026 | Upcoming |
| AIPAC-003 Phase 3 breast cancer update Interim or enrollment update for Phase 3 efti in metastatic breast cancer | data readout | Speculative | arrow_upwardHigh | 31 Dec 2026 | Upcoming |
| AIPAC-003 Phase III breast cancer update Phase III arm of AIPAC-003 progressing following Phase II enrolment completion Oct 2024; full readout timing not yet publicly guided | data readout | Speculative | arrow_upwardHigh | 31 Dec 2026 | Upcoming |
| PHASE3 data readout — Study of Eftilagimod Alfa (Efti) in Combination With Pembrolizumab and Chemotheropen_in_new Primary completion expected for NCT06726265. Indication: {"Advanced/Metastatic Non-Small Cell Lung Cancer (NSCLC)"} | data readout | Speculative | removeMed | 1 June 2027 | Upcoming |
| PHASE2 data readout — Efti in Patients With Hormone Receptor Positive/HER2-neg Breast Canceropen_in_new Primary completion expected for NCT07102940. Indication: {"Breast Cancer","HER 2 Negative Breast Cancer","HR Positive/HER-2 Negative Breast Cancer","Stage 1-3"} | data readout | Speculative | removeMed | 1 Aug 2028 | Upcoming |
| Update on Phase I Study of IMP761 for Autoimmune Diseasesopen_in_new The single ascending dose (SAD) portion of the first-in-human Phase I study has been successfully completed, with dosing up to 14 mg/kg in healthy participants. IMP761 demonstrated a clear immunosuppressive effect, showing durable inhibition of T-cell-mediated responses after a single administration in participants challenged with a foreign antigen. The multiple ascending dose (MAD) portion is currently ongoing across two dose levels, with completion expected in Q3 2026. | data readout | Confirmed | removeMed | 18 Mar 2026 | Completed |
| Results posted — Combination Study With Soluble LAG-3 Fusion Protein Eftilagimod Alpha (IMP321) aopen_in_new Results available at https://clinicaltrials.gov/study/NCT03625323 | data readout | Confirmed | High |
| 8 Apr 2026 |
| Completed |
| Results posted — Immunotherapy of HLA-A2 Positive Stage II-IV Melanoma Patientsopen_in_new Results available at https://clinicaltrials.gov/study/NCT01308294 | data readout | Confirmed | arrow_upwardHigh | 8 Apr 2026 | Completed |
| Results posted — Combination Study With Soluble LAG-3 Fusion Protein Eftilagimod Alpha (IMP321) aopen_in_new Results available at https://clinicaltrials.gov/study/NCT03625323 | data readout | Confirmed | arrow_upwardHigh | 13 Apr 2026 | Completed |
| Results posted — Immunotherapy of HLA-A2 Positive Stage II-IV Melanoma Patientsopen_in_new Results available at https://clinicaltrials.gov/study/NCT01308294 | data readout | Confirmed | arrow_upwardHigh | 13 Apr 2026 | Completed |
| Eftilagimod Alfa (efti) FDA — Immutep receives FDA ODD for Efti in Soft Tissue Sarcomaopen_in_new The FDA granted Orphan Drug Designation to eftilagimod alfa for the treatment of soft tissue sarcoma, a rare cancer affecting fewer than 200,000 people in the United States. This designation is supported by encouraging Phase II EFTISARC-NEO trial data showing a median tumour hyalinization/fibrosis of 51.5%, significantly exceeding the pre-specified target of 35%. | regulatory decision | Confirmed | removeMed | 14 Apr 2026 | Completed |