{"id":10597,"date":"2026-08-11T05:11:00","date_gmt":"2026-08-10T22:11:00","guid":{"rendered":"https:\/\/www.globenewswire.com\/news-release\/2026\/08\/10\/3342348\/0\/en\/portnoy-law-firm-announces-class-action-on-behalf-of-capricor-therapeutics-inc-investors.html3342348"},"modified":"2026-08-11T05:13:57","modified_gmt":"2026-08-10T22:13:57","slug":"portnoy-law-firm-announces-class-action-on-behalf-of-capricor-therapeutics-inc-investors","status":"publish","type":"post","link":"https:\/\/cryptoinsider.asia\/vi\/portnoy-law-firm-announces-class-action-on-behalf-of-capricor-therapeutics-inc-investors\/","title":{"rendered":"Portnoy Law Firm Announces Class Action on Behalf of Capricor Therapeutics, Inc. Investors"},"content":{"rendered":"\n<p>LOS ANGELES, Aug. 10, 2026 (GLOBE NEWSWIRE) &#8212; <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=y7YcxvKr9xHuuHzB3fQ-XwhavwNWHgPtoWcVYa6SYYCE5SMC-HSWn5Vs4ajA3UmcKoKqHjtNVl6VdjiIfCz37HpkeKLXKkRnygSr7selnySo3TSdL_xkTZjLgKGqv8Wo\" rel=\"nofollow\" target=\"_blank\" title><u>The Portnoy Law Firm<\/u><\/a> advises Capricor Therapeutics, Inc., (\u201cCapricor\u201d or the &#8220;Company&#8221;) (NASDAQ: CAPR) investors of a class action on behalf of investors that bought securities between December 17, 2025 and July 26, 2026, inclusive (the \u201cClass Period\u201d). Capricor investors have until September 28, 2026 to file a lead plaintiff motion.<\/p>\n<p>Investors are encouraged to contact attorney <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=GyPkfhFajY-Xz5pvKSsHH6cVF9ynBn-mqIiB2GcR1UnVWIZCwvpV9ncRON1uUsXIekdqct1s4wfJUHbBrYh3G_H4oMPG9y82yh66FLlr9MO2s3N1DSLATqmQ6y3qwXgB\" rel=\"nofollow\" target=\"_blank\" title><u>Lesley F. Portnoy<\/u><\/a>,&nbsp;by phone 310-692-8883 or <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=KIDx29Bi4p8ZTznhyR2idsmRTcmD4NHaprbv_FvcwSqXIOUfaX7j_U8YlDp8EU1GGR8209W3rGVUSdf-UYkHNx4WcH_5VxxjxXGfsOjXyAw=\" rel=\"nofollow\" target=\"_blank\" title><u>email<\/u><\/a>: lesley@portnoylaw.com, to discuss their legal rights, or join the case via <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=vGHOQlXfyJncb8FWEKPvIvTSN_916MXtbhP60DL09tMWjMFloM19Vqvyv1p3z2KpVtyImnfcOJA6_NAmioAbJleXCJAkhEJqHYBzctIh9m-J9lZjlPj8ZXYzyRNwjFnvzapQhac_UCqwmibotGbwbNRUkW4EJv90gbKB5Fs64Zc=\" rel=\"nofollow\" target=\"_blank\" title><u>https:\/\/portnoylaw.com\/capricor-therapeutics-inc<\/u><\/a>. The Portnoy Law Firm can provide a complimentary case evaluation and discuss investors\u2019 options for pursuing claims to recover their losses.<\/p>\n<p>Capricor is a biotechnology company focused on the development of cell and exosome-based therapeutics for the treatment of Duchenne muscular dystrophy, a rare genetic disorder characterized by progressive muscle degeneration and premature death. Its lead product candidate is Deramiocel, a cell therapy to address cardiac and skeletal muscle complications associated with Duchenne muscular dystrophy.<\/p>\n<p>The&nbsp;<em>Capricor&nbsp;<\/em>class action lawsuit alleges that defendants throughout the Class Period made false and\/or misleading statements and\/or failed to disclose that: (i) Capricor adopted changes to the pre-specified statistical analysis plan used to analyze clinical data for Deramiocel; (ii) the FDA had not agreed to those changes before Capricor resubmitted the Deramiocel Biologics License Application (\u201cBLA\u201d); (iii) as a result, there was a significant risk that the FDA could conclude the clinical results did not provide substantial evidence of effectiveness of Deramiocel; and (iv) as a result of the foregoing, there was a substantial risk to regulatory approval of Deramiocel for the treatment of Duchenne muscular dystrophy.<\/p>\n<p>On July 27, 2026, before the market opened, the FDA allegedly released briefing documents ahead of its July 29 advisory committee meeting for the BLA.&nbsp; According to the complaint, the briefing documents explained that Capricor made changes to the pre-specified statistical analysis plan (\u201cSAP\u201d) and that the final version \u201cwas not submitted to FDA for review prior to BLA submission and was not discussed and consequently not agreed upon.\u201d&nbsp; The final version of the statistical analysis plan was allegedly created one day before the data was unblinded, and the FDA commented that the \u201cFDA does not consider the conversion of raw change to percent change and then back to raw change to have been scientifically justified, as it adds complexity and reduces accuracy.\u201d&nbsp; The FDA allegedly further stated that it \u201cconsiders [Capricor\u2019s] analyses based on the post-study SAP versions to be post-hoc and exploratory.\u201d&nbsp; The complaint further alleges that the briefing documents concluded \u201cthe benefit-risk assessment for [D]eramiocel appears unfavorable in the absence of evidence of effectiveness.\u201d<\/p>\n<p>That same day, Capricor allegedly provided \u201can update,\u201d stating that \u201c\u2018Capricor has engaged fully and transparently with the FDA throughout the review process\u2019\u201d and that \u201c\u2018[i]t is critical to understand that the post-hoc analyses in the FDA\u2019s briefing materials rely on SAP version 1.1, an unsigned incomplete internal draft which became obsolete with the addition of cohort B and did not include content specifically requested by the FDA.\u2019\u201d&nbsp; The&nbsp;<em>Capricor&nbsp;<\/em>class action lawsuit further alleges that Cantor Fitzgerald published an investor note that same day, stating the FDA\u2019s \u201cbriefing documents paint an ugly picture\u201d and \u201craise several concerns and make allegations about the integrity of data collecting.\u201d&nbsp; On this news, the price of Capricor stock fell 64%, according to the complaint.<\/p>\n<p>On July 29, 2026, the advisory committee allegedly met to discuss the Deramiocel BLA.&nbsp; The next day, Medscape reported that the panel relied on SAP version 1.1 as the \u201cprespecified plan\u201d and, in a non-binding 9-3 vote, the panel \u201cconcluded that the available evidence does not support the efficacy of deramiocel for treating DMD-associated cardiomyopathy.\u201d&nbsp; On this news, the price of Capricor stock fell 36%, according to the complaint.<\/p>\n<p>The Portnoy Law Firm represents investors in pursuing claims caused by corporate wrongdoing. The Firm\u2019s founding partner has recovered over $5.5 billion for aggrieved investors. Attorney advertising. Prior results do not guarantee similar outcomes.<\/p>\n<p>Lesley F. Portnoy, Esq.<br \/>Admitted CA, NY and TX Bar<br \/><a href=\"https:\/\/www.globenewswire.com\/Tracker?data=u1UGuv7bPaxGHW5E7rjbmKuALq-pi4xJT-NLgaJFriElYFElYknpH_VXeAvKeRmQzIA2lrloxnKgTl2NWnJIt-w7jwijzBSvwNU82Wwn94Q=\" rel=\"nofollow\" target=\"_blank\" title><u>lesley@portnoylaw.com<\/u><\/a><br \/>310-692-8883<br \/>www.portnoylaw.com<\/p>\n<p>Attorney Advertising<\/p>\n<p><img decoding=\"async\" alt src=\"https:\/\/ml.globenewswire.com\/media\/Zjc2MTlkMDItOTgzYi00M2JkLThkNmQtYzI0NGZhMTNjNDVmLTEyMDcwODAtMjAyNi0wOC0xMC1lbg==\/tiny\/Portnoy-Law.png\" referrerpolicy=\"no-referrer-when-downgrade\">  <\/p>\n","protected":false},"excerpt":{"rendered":"<p> LOS ANGELES, Aug. 10, 2026 (GLOBE NEWSWIRE) &#8212; The Portnoy Law Firm advises Capricor Therapeutics, Inc., (\u201cCapricor\u201d or the &#8220;Company&#8221;) (NASDAQ: CAPR) investors of a class action on behalf of investors that bought securities between December 17, 2025 and July 26, 2026, inclusive (the \u201cClass Period\u201d). Capricor investors have until September 28, 2026 to file a lead plaintiff motion. Investors are encouraged to contact attorney Lesley F. Portnoy,\u00a0by phone 310-692-8883 or email: lesley@portnoylaw.com, to discuss their legal rights, or join&#8230;<\/p>\n","protected":false},"author":1,"featured_media":10598,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_lmt_disableupdate":"","_lmt_disable":"","_jetpack_newsletter_access":"","_jetpack_dont_email_post_to_subs":false,"_jetpack_newsletter_tier_id":0,"_jetpack_memberships_contains_paywalled_content":false,"_jetpack_feature_clip_id":0,"_jetpack_memberships_contains_paid_content":false,"footnotes":"","jetpack_publicize_message":"","jetpack_publicize_feature_enabled":true,"jetpack_social_post_already_shared":true,"jetpack_social_options":{"image_generator_settings":{"template":"highway","default_image_id":0,"font":"","enabled":false},"version":2},"jetpack_post_was_ever_published":false},"categories":[75,1406],"tags":[],"class_list":["post-10597","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-business","category-globenewswire"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v28.2 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Portnoy Law Firm Announces Class Action on Behalf of Capricor Therapeutics, Inc. Investors<\/title>\n<meta name=\"description\" content=\"LOS ANGELES, Aug. 10, 2026 (GLOBE NEWSWIRE) -- The Portnoy Law Firm advises Capricor Therapeutics, Inc., (\u201cCapricor\u201d or the &quot;Company&quot;) (NASDAQ: CAPR) investors of a class action on behalf of investors that bought securities between December 17, 2025 and July 26, 2026, inclusive (the \u201cClass Period\u201d). Capricor investors have until September 28, 2026 to file a lead plaintiff motion. Investors are encouraged to contact attorney Lesley F. 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