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Wilsons Advisory

External broker reports(aggregated public sources)

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Equity Bottom-Up

Clarity Pharmaceuticals Ltd / Equity Bottom-Up

<ul>
<li>Clarity have announced that PROPELLER, their Phase I diagnostic trial assessing 64Cu-SAR- bisPSMA in detecting prostate cancer, has met all primary and secondary endpoints.</li>
<li>As outlined in our most recent note, this trial represents a significant de-risking point for the company, validating the use of their SAR copper platform, and, transitioning the company into a pivotal trial stage in 2023, with Clarity confirming start of a pivotal Phase III for this diagnostic asset next year.</li>
<li>Full data on 64Cu SAR-bisPSMA will be released at the American Society of Clinical Oncology (ASCO) Genitourinary (GU) Symposium in February 2023.</li>
</ul>
<p><em>Content is external broker report sourced from online content aggregator through publicly available sources and is displayed below for general informational purposes only. Refer full disclaimer below.</em></p>


Clarity have announced that PROPELLER, their Phase I diagnostic trial assessing 64Cu-SAR- bisPSMA in detecting prostate cancer, has met all primary and secondary endpoints.
As outlined in our most recent note, this trial represents a significant de-risking point for the company, validating the use of their SAR copper platform, and, transitioning the company into a pivotal trial stage in 2023, with Clarity confirming start of a pivotal Phase III for this diagnostic asset next year.
Full data on 64Cu SAR-bisPSMA will be released at the American Society of Clinical Oncology (ASCO) Genitourinary (GU) Symposium in February 2023.

Content is external broker report sourced from online content aggregator through publicly available sources and is displayed below for general informational purposes only. Refer full disclaimer below.

Clarity Pharmaceuticals (CU6) - Propulsion of Value with Positive Topline Results

<div><div><div><ul><li>We maintain our OVERWEIGHT rating on Clarity Pharmaceuticals with a revised price target of $1.22/sh.</li><li>We view the upcoming release of Clarity’s Phase I/II PROPELLER trial results for their 64Cu-SAR-bisPSMA in prostate cancer diagnosis as a de-risking event, with clear signals towards a positive outcome.</li><li>The readout represents an important step in Clarity’s development to a) verify the efficacy of their coupled SAR-copper technology; and b) transition the company into ‘pivotal- trial stage’, as Clarity move closer towards unlocking revenue to support longer-term programs. </li></ul></div></div></div><p><em>Content is external broker report sourced from online content aggregator through publicly available sources and is displayed below for general informational purposes only. Refer full disclaimer below.</em></p>

We maintain our OVERWEIGHT rating on Clarity Pharmaceuticals with a revised price target of $1.22/sh.We view the upcoming release of Clarity’s Phase I/II PROPELLER trial results for their 64Cu-SAR-bisPSMA in prostate cancer diagnosis as a de-risking event, with clear signals towards a positive outcome.The readout represents an important step in Clarity’s development to a) verify the efficacy of their coupled SAR-copper technology; and b) transition the company into ‘pivotal- trial stage’, as Clarity move closer towards unlocking revenue to support longer-term programs. Content is external broker report sourced from online content aggregator through publicly available sources and is displayed below for general informational purposes only. Refer full disclaimer below.

Clarity Pharmaceuticals (CU6) - PROPELLED to Upgrade

<ul><li><span data-sheets-value='{"1":2,"2":"Content is external broker report sourced from online content aggregator through publicly available sources and is displayed below for general informational purposes only. Refer full disclaimer below."}' data-sheets-userformat='{"2":33281,"3":{"1":0},"12":0,"18":1}'>Over the weekend, in a 16-0 vote, the FDA’s Oncologic Drug Advisory Committee (ODAC) decided Y-mAbs therapeutics’ omburtamab (commercialized as OMBLASTYS®) had not provided sufficient evidence to conclude improvement in overall survival for the treatment of central nervous system (CNS)/leptomeningeal metastasis from paediatric neuroblastoma. </span></li><li><span data-sheets-value='{"1":2,"2":"Content is external broker report sourced from online content aggregator through publicly available sources and is displayed below for general informational purposes only. Refer full disclaimer below."}' data-sheets-userformat='{"2":33281,"3":{"1":0},"12":0,"18":1}'>The PDUFA date had been set for November 30 2022, following BLA submission in April this year. </span></li><li><span data-sheets-value='{"1":2,"2":"Content is external broker report sourced from online content aggregator through publicly available sources and is displayed below for general informational purposes only. Refer full disclaimer below."}' data-sheets-userformat='{"2":33281,"3":{"1":0},"12":0,"18":1}'>Omburtamab represented the potential expansion of Y-mAb’s neuroblastoma treatment offering following FDA approval of their DANYELZATM drug in 2020. </span></li></ul><p><em>Content is external broker report sourced from online content aggregator through publicly available sources and is displayed below for general informational purposes only. Refer full disclaimer below.</em></p>

Over the weekend, in a 16-0 vote, the FDA’s Oncologic Drug Advisory Committee (ODAC) decided Y-mAbs therapeutics’ omburtamab (commercialized as OMBLASTYS®) had not provided sufficient evidence to conclude improvement in overall survival for the treatment of central nervous system (CNS)/leptomeningeal metastasis from paediatric neuroblastoma. The PDUFA date had been set for November 30 2022, following BLA submission in April this year. Omburtamab represented the potential expansion of Y-mAb’s neuroblastoma treatment offering following FDA approval of their DANYELZATM drug in 2020. Content is external broker report sourced from online content aggregator through publicly available sources and is displayed below for general informational purposes only. Refer full disclaimer below.

Clarity Pharmaceuticals (CU6) - FDA No-Go for Y-MAb’s Neuroblastoma Drug

<div><div><div><ul><li>We initiate coverage on Clarity Pharmaceuticals with an OVERWEIGHT rating and $0.82/sh risked PT.</li><li>Clarity has played a clever and patient game in nuclear medicine, ensuring the two most important factors for success, are in place.</li><li>Those being: a) technology which secures copper (64Cu &amp; 67Cu) without leakage and b) commercial production of 67Cu for use in therapy. </li></ul></div></div></div><p><em>Content is external broker report sourced from online content aggregator through publicly available sources and is displayed below for general informational purposes only. Refer full disclaimer below.</em></p>

We initiate coverage on Clarity Pharmaceuticals with an OVERWEIGHT rating and $0.82/sh risked PT.Clarity has played a clever and patient game in nuclear medicine, ensuring the two most important factors for success, are in place.Those being: a) technology which secures copper (64Cu &amp; 67Cu) without leakage and b) commercial production of 67Cu for use in therapy. Content is external broker report sourced from online content aggregator through publicly available sources and is displayed below for general informational purposes only. Refer full disclaimer below.

Clarity Pharmaceuticals (CU6) - Bringing Clarity to Radiopharmaceuticals

Australia

Clarity Pharmaceuticals Limited operates as a radio-pharmaceutical company. The Company focuses on the developing targeted therapies for the treatment of cancer and other serious diseases. Clarity Pharmaceuticals serves customers worldwide.

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Clarity Pharmaceuticals Ltd (CU6 AU)

Clarity Pharmaceuticals (CU6) - Propulsion of Value with Positive Topline Results

Clarity have announced that PROPELLER, their Phase I diagnostic trial assessing 64Cu-SAR- bisPSMA in detecting prostate cancer, has met all primary...

Wilsons Advisory

Clarity Pharmaceuticals (CU6) - PROPELLED to Upgrade

We view the upcoming release of Clarity’s Phase I/II PROPELLER trial results for their 64Cu-SAR-bisPSMA in prostate cancer diagnosis as a de...

Wilsons Advisory

Clarity Pharmaceuticals (CU6) - FDA No-Go for Y-MAb’s Neuroblastoma Drug

The negative outcome isn’t the first for Y-mAbs. The BLA for omburtamab was originally submitted to the FDA in August 2020.

Wilsons Advisory

Clarity Pharmaceuticals (CU6) - Bringing Clarity to Radiopharmaceuticals

Clarity has played a clever and patient game in nuclear medicine, ensuring the two most important factors for success, are in place.

Wilsons Advisory

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