Press Releases April 7, 2026 08:00 PM

Radiopharm Theranostics Advances to Cohort 3 in 177Lu-RAD202 Phase 1 Dose Escalating Clinical Trial

Radiopharm Theranostics progresses to next dose cohort in Phase 1 trial of targeted radiotherapeutic for HER2-positive solid tumors

By Jordan Park RADX
Radiopharm Theranostics Advances to Cohort 3 in 177Lu-RAD202 Phase 1 Dose Escalating Clinical Trial
RADX

Radiopharm Theranostics announced advancement to Cohort 3 at a 130mCi dose in its Phase 1 HEAT clinical trial of 177Lu-RAD202, a radiopharmaceutical targeting HER2-positive advanced solid tumors, following a positive safety review by the Data Safety and Monitoring Committee. The trial remains on track for completion of dose escalation by the end of 2026.

Key Points

  • The Data Safety and Monitoring Committee endorsed escalation to a higher dose level (130mCi) for RAD202 in the Phase 1 trial, indicating a favorable safety profile.
  • RAD202 is a proprietary single-domain monoclonal antibody targeting HER2-positive cancers, including breast and other solid tumors, addressing a significant unmet medical need in oncology.
  • The clinical program is supported by a pipeline spanning multiple platforms, with trials across solid tumor types, highlighting Radiopharm's focus on innovative radiopharmaceutical therapeutics.
  • Impacted sectors include biotechnology, oncology therapeutics, and the broader healthcare and pharmaceutical markets.

SYDNEY, April 08, 2026 (GLOBE NEWSWIRE) -- Radiopharm Theranostics (ASX: RAD, Nasdaq: RADX, “Radiopharm” or the “Company”), a clinical-stage biopharmaceutical company focused on developing innovative oncology radiopharmaceuticals for areas of high unmet medical need, today announced that it has received a positive recommendation from the Data Safety and Monitoring Committee (DSMC) to advance its clinical-stage radiotherapeutic asset, 177Lu-RAD202 (RAD202), to the next dose level of 130mCi in the Phase 1 ‘HEAT’ clinical trial in patients with Human Epidermal Growth Factor Receptor 2 (HER2)-positive advanced solid tumors1. The DSMC is a multidisciplinary committee that conducts detailed reviews of study data, discusses potential safety events and provides recommendations regarding trial continuation.

“We are encouraged by the rapid progress of the Phase 1 ‘HEAT’ trial of RAD202, as it underscores the favorable safety profile, allowing us to accelerate the dose escalation from Cohort 2 to Cohort 3.” said Riccardo Canevari, CEO and Managing Director of Radiopharm Theranostics. “Considering the current progress and the strong execution, we remain on track to complete the Phase 1 dose escalation by the end of 2026.”

The Phase 1 ‘HEAT’ study is currently being conducted at clinical centers across Australia. The announcement of the previous dose level in this study of 75mCi was released on 1 October 2025.

About 177Lu-RAD202:

RAD202 is a proprietary single-domain monoclonal antibody (sdAb) that targets the Human Epidermal Growth Factor Receptor 2 (HER2)-positive expression in advanced solid tumors. HER2 is overexpressed in breast cancer and several other solid tumors and represents a validated target in oncology. In a previous diagnostic study of ten HER2-positive breast cancer patients, RAD202 demonstrated clinical proof-of-concept and had positive safety and biodistribution.

About Radiopharm Theranostics

Radiopharm Theranostics is a clinical stage radiotherapeutics company developing a world-class platform of innovative radiopharmaceutical products for diagnostic and therapeutic applications in areas of high unmet medical need. Radiopharm is listed on ASX (RAD) and on NASDAQ (RADX). The company has a pipeline of distinct and highly differentiated platform technologies spanning peptides, small molecules and monoclonal antibodies for use in cancer. The clinical program includes one Phase 2 and five Phase 1 trials in a variety of solid tumor cancers including lung, breast, prostate and brain. Learn more at radiopharmtheranostics.com.

Authorized on behalf of the Radiopharm Theranostics Board of Directors by Executive Chairman Paul Hopper.

For more information:

Investors:
Riccardo Canevari
CEO & Managing Director
P: +1 862 309 0293
E: [email protected]

Anne Marie Fields
Precision AQ (formerly Stern IR)
E: [email protected]

Media:
Matt Wright
NWR Communications
P: +61 451 896 420
E: [email protected]

Follow Radiopharm Theranostics:
Website – https://radiopharmtheranostics.com/
X – https://x.com/TeamRadiopharm  
LinkedIn – https://www.linkedin.com/company/radiopharm-theranostics/
InvestorHub – https://investorhub.radiopharmtheranostics.com/

1 clinicaltrials.gov/study/NCT06824155


Risks

  • Clinical trial outcomes beyond safety, such as efficacy and longer-term side effects, remain uncertain until further phases are completed.
  • Regulatory approvals and market adoption may delay commercial availability and revenue generation from RAD202.
  • Competition from other HER2-targeted therapies and alternative cancer treatments could impact market share and product success.

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