Phase 1AGENNCT05318469

Ivermectin in Combination With Balstilimab or Pembrolizumab in Patients With Metastatic Triple Negative Breast Cancer FDA Decision: Agenus Inc (AGEN)

Decision Date
October 1, 2026

Drug Overview

Drug / TherapyIvermectin in Combination With Balstilimab or Pembrolizumab in Patients With Metastatic Triple Negative Breast Cancer
Indication
Decision TypePhase 1
Trial PhasePhase 1
ClinicalTrials.govNCT05318469

Company Overview

Agenus Inc (AGEN) operates in the Immuno-Oncology sector. The current BTS Score is 69 (Grade: B).

Dilution Risk Assessment

Biotech companies frequently raise capital through secondary offerings, ATM programs, and convertible notes. Before or after major FDA decisions, dilution events are common. Understanding a company's dilution history is critical for managing risk around catalyst dates.

Frequently Asked Questions

Q:When is the Phase 1 date for Ivermectin in Combination With Balstilimab or Pembrolizumab in Patients With Metastatic Triple Negative Breast Cancer?

The Phase 1 date for Ivermectin in Combination With Balstilimab or Pembrolizumab in Patients With Metastatic Triple Negative Breast Cancer by Agenus Inc (AGEN) is scheduled for October 1, 2026. This is the target date for the FDA to make a decision on this application.

Q:What is Ivermectin in Combination With Balstilimab or Pembrolizumab in Patients With Metastatic Triple Negative Breast Cancer used for?

Ivermectin in Combination With Balstilimab or Pembrolizumab in Patients With Metastatic Triple Negative Breast Cancer is being developed by Agenus Inc for the treatment of its target indication. It is currently in Phase 1 clinical trials.

Q:What happens if Ivermectin in Combination With Balstilimab or Pembrolizumab in Patients With Metastatic Triple Negative Breast Cancer gets FDA approval?

If Ivermectin in Combination With Balstilimab or Pembrolizumab in Patients With Metastatic Triple Negative Breast Cancer receives FDA approval, Agenus Inc (AGEN) would be able to market the drug in the United States for its target indication. This typically leads to significant stock price movement for biotech companies. Investors should monitor the Phase 1 date closely.

Q:What is the dilution risk for AGEN?

Biotech companies often raise capital through share offerings, which can dilute existing shareholders. You can check the current dilution risk for AGEN on DilutionWatch at dilutionwatch.com/stock/AGEN.html.

Q:Where can I find more information about Agenus Inc?

You can view the full BiotechSign company profile for Agenus Inc (AGEN) at biotechsign.com/app/company/AGEN, which includes the BTS Score, signal history, clinical trial data, and insider trading activity.

Disclaimer

This page is for informational purposes only and does not constitute investment advice. FDA decision dates are subject to change. Clinical trial outcomes are inherently uncertain. Biotech stocks are highly volatile — past performance does not guarantee future results. Always consult a qualified financial advisor before making investment decisions. BiotechSign is not a registered investment advisor.