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   <title>Creative Medical completes enrollment in ADAPT back pain trial</title>
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&lt;p&gt;Creative Medical Technology Holdings (NASDAQ: CELZ) announced that all patients have been enrolled and treated across its FDA-cleared ADAPT clinical trial evaluating CELZ-201, also known as Olastrocel, for chronic lower back pain associated with degenerative disc disease, including participants in an opioid expansion cohort cleared by the FDA in June 2026.&lt;/p&gt;

&lt;p&gt;Olastrocel is a perinatal tissue-derived, allogeneic regenerative cell therapy administered through a minimally invasive, ultrasound-guided intramuscular procedure. The ADAPT trial was designed to assess safety, tolerability and preliminary efficacy of the therapy.&lt;/p&gt;

&lt;p&gt;Previously reported interim 180-day data showed a mean improvement in functional disability of 15.3 percentage points, with approximately 79%</description>
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   <title>Creative Medical completes enrollment in ADAPT back pain trial</title>
   <link>http://www.streetinsider.com/FDA/Creative+Medical+completes+enrollment+in+ADAPT+back+pain+trial/26954011.html</link>
   <description>

&lt;p&gt;Creative Medical Technology Holdings (NASDAQ: CELZ) announced that all patients have been enrolled and treated across its FDA-cleared ADAPT clinical trial evaluating CELZ-201, also known as Olastrocel, for chronic lower back pain associated with degenerative disc disease, including participants in an opioid expansion cohort cleared by the FDA in June 2026.&lt;/p&gt;

&lt;p&gt;Olastrocel is a perinatal tissue-derived, allogeneic regenerative cell therapy administered through a minimally invasive, ultrasound-guided intramuscular procedure. The ADAPT trial was designed to assess safety, tolerability and preliminary efficacy of the therapy.&lt;/p&gt;

&lt;p&gt;Previously reported interim 180-day data showed a mean improvement in functional disability of 15.3 percentage points, with approximately 79%</description>
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   <title>Creative Medical completes enrollment in ADAPT back pain trial</title>
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   <description>

&lt;p&gt;Creative Medical Technology Holdings (NASDAQ: CELZ) announced that all patients have been enrolled and treated across its FDA-cleared ADAPT clinical trial evaluating CELZ-201, also known as Olastrocel, for chronic lower back pain associated with degenerative disc disease, including participants in an opioid expansion cohort cleared by the FDA in June 2026.&lt;/p&gt;

&lt;p&gt;Olastrocel is a perinatal tissue-derived, allogeneic regenerative cell therapy administered through a minimally invasive, ultrasound-guided intramuscular procedure. The ADAPT trial was designed to assess safety, tolerability and preliminary efficacy of the therapy.&lt;/p&gt;

&lt;p&gt;Previously reported interim 180-day data showed a mean improvement in functional disability of 15.3 percentage points, with approximately 79%</description>
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   <title>Creative Medical completes enrollment in ADAPT back pain trial</title>
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   <description>

&lt;p&gt;Creative Medical Technology Holdings (NASDAQ: CELZ) announced that all patients have been enrolled and treated across its FDA-cleared ADAPT clinical trial evaluating CELZ-201, also known as Olastrocel, for chronic lower back pain associated with degenerative disc disease, including participants in an opioid expansion cohort cleared by the FDA in June 2026.&lt;/p&gt;

&lt;p&gt;Olastrocel is a perinatal tissue-derived, allogeneic regenerative cell therapy administered through a minimally invasive, ultrasound-guided intramuscular procedure. The ADAPT trial was designed to assess safety, tolerability and preliminary efficacy of the therapy.&lt;/p&gt;

&lt;p&gt;Previously reported interim 180-day data showed a mean improvement in functional disability of 15.3 percentage points, with approximately 79%</description>
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   <title>Creative Medical completes enrollment in ADAPT back pain trial</title>
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   <description>

&lt;p&gt;Creative Medical Technology Holdings (NASDAQ: CELZ) announced that all patients have been enrolled and treated across its FDA-cleared ADAPT clinical trial evaluating CELZ-201, also known as Olastrocel, for chronic lower back pain associated with degenerative disc disease, including participants in an opioid expansion cohort cleared by the FDA in June 2026.&lt;/p&gt;

&lt;p&gt;Olastrocel is a perinatal tissue-derived, allogeneic regenerative cell therapy administered through a minimally invasive, ultrasound-guided intramuscular procedure. The ADAPT trial was designed to assess safety, tolerability and preliminary efficacy of the therapy.&lt;/p&gt;

&lt;p&gt;Previously reported interim 180-day data showed a mean improvement in functional disability of 15.3 percentage points, with approximately 79%</description>
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   <title>Creative Medical completes enrollment in ADAPT back pain trial</title>
   <link>http://www.streetinsider.com/FDA/Creative+Medical+completes+enrollment+in+ADAPT+back+pain+trial/26954011.html</link>
   <description>

&lt;p&gt;Creative Medical Technology Holdings (NASDAQ: CELZ) announced that all patients have been enrolled and treated across its FDA-cleared ADAPT clinical trial evaluating CELZ-201, also known as Olastrocel, for chronic lower back pain associated with degenerative disc disease, including participants in an opioid expansion cohort cleared by the FDA in June 2026.&lt;/p&gt;

&lt;p&gt;Olastrocel is a perinatal tissue-derived, allogeneic regenerative cell therapy administered through a minimally invasive, ultrasound-guided intramuscular procedure. The ADAPT trial was designed to assess safety, tolerability and preliminary efficacy of the therapy.&lt;/p&gt;

&lt;p&gt;Previously reported interim 180-day data showed a mean improvement in functional disability of 15.3 percentage points, with approximately 79%</description>
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   <title>Creative Medical completes enrollment in ADAPT back pain trial</title>
   <link>http://www.streetinsider.com/FDA/Creative+Medical+completes+enrollment+in+ADAPT+back+pain+trial/26954011.html</link>
   <description>

&lt;p&gt;Creative Medical Technology Holdings (NASDAQ: CELZ) announced that all patients have been enrolled and treated across its FDA-cleared ADAPT clinical trial evaluating CELZ-201, also known as Olastrocel, for chronic lower back pain associated with degenerative disc disease, including participants in an opioid expansion cohort cleared by the FDA in June 2026.&lt;/p&gt;

&lt;p&gt;Olastrocel is a perinatal tissue-derived, allogeneic regenerative cell therapy administered through a minimally invasive, ultrasound-guided intramuscular procedure. The ADAPT trial was designed to assess safety, tolerability and preliminary efficacy of the therapy.&lt;/p&gt;

&lt;p&gt;Previously reported interim 180-day data showed a mean improvement in functional disability of 15.3 percentage points, with approximately 79%</description>
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   <title>Creative Medical completes enrollment in ADAPT back pain trial</title>
   <link>http://www.streetinsider.com/FDA/Creative+Medical+completes+enrollment+in+ADAPT+back+pain+trial/26954011.html</link>
   <description>

&lt;p&gt;Creative Medical Technology Holdings (NASDAQ: CELZ) announced that all patients have been enrolled and treated across its FDA-cleared ADAPT clinical trial evaluating CELZ-201, also known as Olastrocel, for chronic lower back pain associated with degenerative disc disease, including participants in an opioid expansion cohort cleared by the FDA in June 2026.&lt;/p&gt;

&lt;p&gt;Olastrocel is a perinatal tissue-derived, allogeneic regenerative cell therapy administered through a minimally invasive, ultrasound-guided intramuscular procedure. The ADAPT trial was designed to assess safety, tolerability and preliminary efficacy of the therapy.&lt;/p&gt;

&lt;p&gt;Previously reported interim 180-day data showed a mean improvement in functional disability of 15.3 percentage points, with approximately 79%</description>
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   <title>Creative Medical Technology Holdings Successfully Completes Enrollment and Treatment Across Entire FDA-Cleared ADAPT Trial, Including Opioid Cohort, Advancing CELZ-201 / Olastrocel Toward RMAT Evaluat</title>
   <link>http://www.streetinsider.com/Press+Releases/Creative+Medical+Technology+Holdings+Successfully+Completes+Enrollment+and+Treatment+Across+Entire+FDA-Cleared+ADAPT+Trial%2C+Including+Opioid+Cohort%2C+Advancing+CELZ-201++Olastrocel+Toward+RMAT+Evaluat/26954008.html</link>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;All patients enrolled and treated across original and FDA-cleared expansion cohorts&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Positive safety and early efficacy signals continue to support late-stage development planning for Olastrocel in chronic lower back pain&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;With enrollment and treatment completed, ADAPT-related clinical execution expenses are expected to decrease as the program transitions into follow-up, data maturation and regulatory planning&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Company believes reduced enrollment- and treatment-related expenditures should help preserve capital, extend operating runway and support continued Phase 3 preparation without the immediate need for additional fundraising&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Company remains fully engaged in patient follow-up, data collection, RMAT</description>
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   <link>http://www.streetinsider.com/Press+Releases/Creative+Medical+Technology+Holdings+Successfully+Completes+Enrollment+and+Treatment+Across+Entire+FDA-Cleared+ADAPT+Trial%2C+Including+Opioid+Cohort%2C+Advancing+CELZ-201++Olastrocel+Toward+RMAT+Evaluat/26954008.html</link>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;All patients enrolled and treated across original and FDA-cleared expansion cohorts&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Positive safety and early efficacy signals continue to support late-stage development planning for Olastrocel in chronic lower back pain&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;With enrollment and treatment completed, ADAPT-related clinical execution expenses are expected to decrease as the program transitions into follow-up, data maturation and regulatory planning&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Company believes reduced enrollment- and treatment-related expenditures should help preserve capital, extend operating runway and support continued Phase 3 preparation without the immediate need for additional fundraising&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Company remains fully engaged in patient follow-up, data collection, RMAT</description>
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   <title>Creative Medical Technology Holdings Successfully Completes Enrollment and Treatment Across Entire FDA-Cleared ADAPT Trial, Including Opioid Cohort, Advancing CELZ-201 / Olastrocel Toward RMAT Evaluat</title>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;All patients enrolled and treated across original and FDA-cleared expansion cohorts&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Positive safety and early efficacy signals continue to support late-stage development planning for Olastrocel in chronic lower back pain&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;With enrollment and treatment completed, ADAPT-related clinical execution expenses are expected to decrease as the program transitions into follow-up, data maturation and regulatory planning&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Company believes reduced enrollment- and treatment-related expenditures should help preserve capital, extend operating runway and support continued Phase 3 preparation without the immediate need for additional fundraising&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Company remains fully engaged in patient follow-up, data collection, RMAT</description>
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