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Presentation to Extraordinary General Meeting

Key Takeaway: Radiopharm Theranostics has announced the initiation of a Phase 1/2a clinical study for BetaBart (RV-01) and has received IND approval from the US FDA. The company has also shared positive clinical updates across four of its programs. This marks a significant step forward in their therapeutic development efforts.

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POSITIVE FACTORS

  • Radiopharm Theranostics has initiated a Phase 1/2a clinical study.
  • The company received IND approval from the US FDA.
  • Positive updates were provided across four clinical programs.

Full Press Release Details

• Announcements
• August 14, 2024
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Radiopharm Theranostics Doses First Patient in Phase 1/2a ClinicalStudy of BetaBart (RV-01)

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Radiopharm Theranostics Provides Positive Clinical Updates Across Four Programs

CLINICAL UPDATE AND CAPITAL RAISING OCTOBER 20th, 2025

Radiopharm Theranostics Receives IND approval from US FDA to Initiate Phase I Therapeutic Clinical Study to target B7H3 with Betabart (RV-01)

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Frequently Asked Questions

What is the BetaBart clinical study about?

The BetaBart clinical study is a Phase 1/2a trial initiated by Radiopharm Theranostics.

When did Radiopharm receive FDA approval?

Radiopharm received IND approval from the US FDA to initiate the study.

What updates were provided by Radiopharm?

Radiopharm provided positive clinical updates across four of its programs.

Last updated: Aug 14, 2024