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RAD Presentation March 2026

Key Takeaway: Radiopharm Theranostics has made significant progress with its BetaBart (RV-01) program, having dosed the first patient in a Phase 1/2a clinical study. The company also received IND approval from the US FDA to initiate this therapeutic study targeting B7H3. Additionally, positive updates were shared across four of their clinical programs, indicating a strong outlook for the company.
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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 clinical updates were provided across four programs.

Full Press Release Details

• Investor Presentations
• March 10, 2026
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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)

Dr. Oliver Sartor Appointed to Radiopharm Scientific Advisory Board

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Frequently Asked Questions

What is the BetaBart (RV-01) study?

The BetaBart (RV-01) study is a Phase 1/2a clinical trial initiated by Radiopharm Theranostics.

What recent approval did Radiopharm receive?

Radiopharm Theranostics received IND approval from the US FDA for the BetaBart study.

When was the first patient dosed in the study?

The first patient in the BetaBart study was dosed in October 2025.

What updates were provided by Radiopharm?

Radiopharm shared positive clinical updates across four of its programs.

Last updated: Mar 10, 2026