RDPTF Radiopharm Theranostics Ltd

BULLISH Impact: 7/10 6-K
Horizon weeks Filed Apr 7, 2026 Processed 2mo ago SEC 0001213900-26-040690
Notable filing: 6-K
Latest settled — T+20d
RDPTF ▲ 0.00% at T+20d
LONG call ✗ call lost 0.00% · α vs SPY -9.78% · entry $0.0200 → $0.0200
Next anchor: T+60d in 22d
Currently $0.0200 · -0.00% from $0.0200 entry
Entry anchored
Apr 7, 2026
via day open
T+1d
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call 0.00% · α -2.54%
$0.0200
settled 2mo ago
T+5d
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call 0.00% · α -5.33%
$0.0200
settled 8w ago
T+20d
0.00%
call 0.00% · α -9.78%
$0.0200
settled 5w ago
T+60d
call — · α —
in 22d

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Executive Summary

Radiopharm Theranostics announced a clinical supply agreement with Siemens Healthineers for RAD101, a novel imaging agent targeting brain metastases. The partnership ensures supply for the upcoming Phase 3 registrational trial in the U.S., following positive interim Phase 2b data showing 90% concordance with MRI and FDA Fast Track Designation.

Actionable Insight

The Siemens partnership de-risks the Phase 3 trial supply chain and validates RAD101's potential. Traders should monitor upcoming topline Phase 2b data in 1H 2026 and progression into Phase 3 as key catalysts. Positive data could drive valuation higher given the large unmet need in brain metastases (300,000 U.S. diagnoses annually).

Key Facts

  • Radiopharm Theranostics (RAD) and Siemens Healthineers signed a clinical supply agreement for RAD101 in the U.S.
  • RAD101 is a novel FASN-targeting PET imaging agent for suspected recurrent brain metastases.
  • Interim Phase 2b data showed 90% concordance (primary endpoint) between RAD101 PET imaging and MRI, with significant and selective tumor uptake in brain metastases.
  • FDA has granted Fast Track Designation for RAD101 to distinguish between recurrent disease and treatment effect in brain metastases.
  • Siemens will radiolabel and distribute 18F-labeled RAD101 to support Radiopharm's upcoming Phase 3 registrational trial in the U.S.
  • Company is listed on ASX (RAD) and NASDAQ (RADX).

Financial Impact

Positive advancement in clinical development with no immediate direct financial impact disclosed; reduces execution risk for Phase 3 trial through established manufacturing and distribution partnership.

clinical progressregulatory pathwaytrial execution risk

Risk Factors

  • Phase 2b topline data not yet fully reported; interim analysis showed positive trend but final results may differ.
  • Phase 3 trial has not yet commenced; regulatory or enrollment delays possible.
  • RAD101 remains investigational; future clinical results may not confirm initial promise.

Market Snapshot

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Documents Analyzed

This report is based on 5 SEC documents filed with EDGAR.

DocumentAccession Number
6-K Filing (Primary)0001213900-26-040690
Document: ea028536301ex99-1.htm0001213900-26-040690
Document: 0001213900-26-040690-index-headers.html0001213900-26-040690
Document: 0001213900-26-040690-index.html0001213900-26-040690
Document: 0001213900-26-040690.txt0001213900-26-040690
8 reports for RDPTF
Performance horizon
0% Hit rate 0 of 3 directional calls best @ T+1· 0.00%Mar 27, 2026
Filters
Rows
Reports for RDPTF — sortable, filterable
Type Now
Jun 3, 2026
6d ago
6-K
NEUTRAL ★ 2/10
$0.0200 $0.0200· 0.00%▼ −0.40%$0.0200 (−0.00%)
May 7, 2026
4w ago
3
NEUTRAL ★ 2/10
$0.0200 $0.0200· 0.00%▼ −0.83%$0.0200 (−0.00%)
Apr 23, 2026
6w ago
6-K
MIXED ★ 5/10
$0.0200 $0.0200· 0.00%▼ −0.78%$0.0200 (−0.00%)
Apr 16, 2026
7w ago
6-K
BULLISH ★ 7/10
$0.0200 $0.0200· 0.00%▼ −1.21%$0.0200 (−0.00%)
Apr 8, 2026
8w ago
6-K
BULLISH ★ 6/10
$0.0200 $0.0200· 0.00%▼ −0.57%$0.0200 (−0.00%)
Apr 7, 2026
9w ago
6-K
BULLISH ★ 7/10
$0.0200 $0.0200· 0.00%▼ −2.54%$0.0200 (−0.00%)
Apr 2, 2026
9w ago
3
NEUTRAL ★ 3/10
$0.0200 $0.0200· 0.00%▼ −0.48%$0.0200 (−0.00%)
Mar 27, 2026
10w ago
6-K
BULLISH ★ 7/10
$0.0200 $0.0200· 0.00%▲ +0.36%$0.0200 (−0.00%)
Showing 8 of 8

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