Follow the Janux Therapeutics, Inc. share price and the full management transaction log of the company, a publicly traded company based in United States. Shares trade on US US, under the authority of SEC (Form 4). Operating in the Healthcare & Pharma sector, Janux Therapeutics, Inc. has logged 90 reports. Market capitalisation: €947.7m. The latest transaction was disclosed on 12 June 2026 (Attribution). Among the most active insiders: Avalon Ventures XI, L.P.. All data is accessible without an account.
Analysts rate Janux Therapeutics, Inc. Strong Buy (bullish), based on 16 analysts. Average price target: US$37.19.
Informational score on this market. Our backtest validates the signal only on 8 EU venues; elsewhere (notably US markets) insider buys historically invert or do not hold. Not a recommendation.
Fundamental view, insider signal, bull and bear case, synthesis.
AI-generated analysis. Opinion, not investment advice. Not backtested. Built from public filings and financials. No price target, no buy or sell recommendation.
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Janux Therapeutics, Inc. is a US-listed clinical-stage biopharmaceutical company trading on the NASDAQ under the ticker JANX. Headquartered in San Diego, California, and incorporated in Delaware in June 2017, the company focuses on next-generation immunotherapies for cancer and, more recently, autoimmune disease. Its strategy is built around proprietary platforms designed to conditionally activate T cells in the tumor microenvironment, with the goal of preserving anti-tumor potency while reducing the systemic toxicity that has limited many earlier immunotherapy approaches. Janux’s core technology stack includes TRACTr (Tumor Activated T Cell Engager), TRACIr (Tumor Activated Immunomodulator), and ARM (Adaptive Immune Response Modulator), which together form the basis of a platform-driven pipeline strategy. From a business perspective, Janux remains a development-stage company with no marketed products and no product revenue to date. Its operating model is centered on R&D, translational work, and early clinical execution. The company’s lead historical program has been JANX007, a PSMA-targeted TRACTr being evaluated in prostate cancer, including metastatic castration-resistant prostate cancer (mCRPC). Janux also advanced JANX008, an EGFR-targeted candidate in multiple solid tumors, while expanding its pipeline with JANX011, the first clinical asset from its ARM platform, and JANX014. The company has also highlighted autoimmune disease as a longer-term expansion opportunity, broadening its addressable market beyond oncology. In 2026, Janux announced discontinuation of the JANX008 clinical program, a reminder that pipeline management remains highly data-dependent in this sector. Competitively, Janux operates in a crowded and scientifically demanding landscape that includes bispecific antibody developers, T-cell engager specialists, and large pharmaceutical companies pursuing similar tumor-directed immune strategies. Its main differentiation thesis is that conditional, tumor-restricted activation can improve the therapeutic window and potentially support more convenient dosing regimens. In that sense, Janux is best viewed as a platform biotech rather than a single-asset company, with value creation dependent on whether its proprietary biology can repeatedly generate clinically meaningful candidates. Geographically, Janux is primarily US-based, with its main headquarters and operational footprint in San Diego, a major biotech hub. Its clinical development and investor communications are also centered on the United States. Recent milestones have been notable: in 2025 and 2026 the company reported multiple pipeline and clinical updates, announced an exclusive worldwide collaboration with Bristol Myers Squibb in January 2026, disclosed a clinical milestone in its Merck collaboration, dosed the first participant in the JANX011 Phase 1 study in February 2026, and later announced the discontinuation of JANX008 in April 2026. For investors, JANX remains a high-risk, high-upside oncology and immunology platform story driven by clinical readouts, partner validation, and disciplined portfolio progression.