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Activity of IMM-1-104 alone or in combination with chemotherapy in RAS-altered pancreatic cancer models

Key Takeaway: The poster presentation on IMM-1-104 highlights its effectiveness in RAS-altered pancreatic cancer models, showing promising results when combined with chemotherapy agents like gemcitabine and paclitaxel. In preclinical models, IMM-1-104 demonstrated superior tumor growth inhibition compared to standard therapies. The ongoing Phase 2a clinical trial is evaluating its efficacy in patients, with initial data expected in 2024.
Price reaction · baseline $2.12 (2024-04-08 close) · hit pre-market · clean, no other IMRX news in the window
day 0 close · peak
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Market Sentiment Analysis

POSITIVE FACTORS

  • IMM-1-104 shows promising combination effects with chemotherapy.
  • Demonstrated greater tumor growth inhibition compared to other treatments.
  • Ongoing Phase 2a trial includes multiple patients with pancreatic cancer.

BiopharmaWatch Analysis

From our catalyst data and publicly available data · not financial advice
Best trade, last catalyst
+41%
120-day peak, hindsight
Typical move
11.4%
average across 8 past catalysts
Cash runway
~36 mo
Minimal dilution risk
Lead asset
IMM-1-104 Monotherapy
Phase 1 · Advanced Solid Tumor

Full Press Release Details

In a poster titled, “Activity of IMM-1-104 alone or in combination with chemotherapy in RAS-altered pancreatic cancer models,” IMM-1-104, gemcitabine (GEM), nab-paclitaxel (PAC), and 5-fluorouracil (5-FU) were evaluated in tumor xenograft models alone or across multiple combinations.
Results:
• IMM-1-104 showed promising combination effects when treated with gemcitabine (GEM), paclitaxel (PAC) or fluorouracil (5FU) in 3D-tumor growth assay (TGA) pancreatic cancer models.
• IMM-1-104 was synergistic with chemotherapy in animal models of pancreatic cancer.
• In a human pancreatic cancer cell line (MIA PaCa-2) tumor xenograft model, IMM-1-104 alone showed greater tumor growth inhibition (TGI) and better durability than any single or combination chemotherapy tested.
• At day 39, antitumor activity (TGI%) was 103% for IMM-1-104 at 125 mg/kg BID PO, 25.2% for GEM at 60 mg/kg IP Q4D, 62.2% for PAC at 10 mg/kg IV Q4D, and 36.6% for 5FU at 50 mg/kg IP Q4D.
In the Phase 2a portion of Immuneering’s ongoing IMM-1-104 Phase 1/2a clinical trial, IMM-1-104 is being evaluated as both monotherapy and in select combinations with approved chemotherapeutic agents. The Phase 2a portion includes five arms, three of which focus on patients with pancreatic cancer. Patients are now on treatment in multiple arms of the ongoing Phase 2a trial, including multiple patients with pancreatic cancer who are being treated with IMM-1-104 in combination with chemotherapy in the first-line setting. The company expects initial data from multiple Phase 2a arms in 2024.

Frequently Asked Questions

What is IMM-1-104?

IMM-1-104 is a therapeutic agent evaluated for its effectiveness in treating pancreatic cancer.

How does IMM-1-104 perform against chemotherapy?

IMM-1-104 showed greater tumor growth inhibition compared to standard chemotherapy agents.

What are the results of the Phase 2a trial?

The Phase 2a trial is ongoing, with initial data expected in 2024.

What combinations were tested with IMM-1-104?

IMM-1-104 was tested alone and in combination with gemcitabine, paclitaxel, and 5-fluorouracil.

Last updated: Apr 9, 2024