{"id":692896,"date":"2022-10-06T08:35:05","date_gmt":"2022-10-06T12:35:05","guid":{"rendered":"https:\/\/www.marketnewsdesk.com\/index.php\/kiromic-biopharma-announces-fda-feedback-from-type-b-pre-ind-meeting-confirms-deltacel-development-strategy\/"},"modified":"2022-10-06T08:35:05","modified_gmt":"2022-10-06T12:35:05","slug":"kiromic-biopharma-announces-fda-feedback-from-type-b-pre-ind-meeting-confirms-deltacel-development-strategy","status":"publish","type":"post","link":"https:\/\/www.marketnewsdesk.com\/index.php\/kiromic-biopharma-announces-fda-feedback-from-type-b-pre-ind-meeting-confirms-deltacel-development-strategy\/","title":{"rendered":"Kiromic BioPharma Announces FDA Feedback from Type B Pre-IND Meeting Confirms Deltacel Development Strategy"},"content":{"rendered":"

<\/p>\n

Kiromic BioPharma Announces FDA Feedback from Type B Pre-IND Meeting Confirms Deltacel Development Strategy <\/b><\/p>\n

Company Reiterates Deltacel is Next Clinical Trial Candidate, with Projected Clinical Trial Launch Expected in Q1 2023<\/i><\/b><\/p>\n

Company is Streamlining Operations to Execute Deltacel-Aligned Development Strategy<\/i><\/b><\/p>\n

HOUSTON–(BUSINESS WIRE<\/a>)–Kiromic BioPharma, Inc. (NASDAQ: KRBP) (\u201cKiromic\u201d or the \u201cCompany\u201d),<\/b> a clinical-stage fully-integrated biotherapeutics company using its proprietary DIAMOND\u00ae<\/sup> artificial intelligence and data mining platform to develop cell and gene therapies with a focus on immuno-oncology, announces it received validating written feedback on October 4, 2022 from the FDA pursuant to its Type B Pre-IND meeting request regarding its Deltacel\u2122 development strategy.\n<\/p>\n

\nThe purpose of the Pre-IND meeting request was to seek alignment with and to obtain FDA guidance on Kiromic\u2019s proposed development strategy about the chemistry, manufacturing, and controls (CMC), nonclinical studies, and clinical study plan for Deltacel\u2122\/KB-GDT for treating subjects with Non-Small Cell Lung Cancer (NSCLC). Kiromic will leverage this FDA Pre-IND written confirmatory feedback and recommendations into a robust IND submission package for a projected clinical trial launch in Q1 2023.\n<\/p>\n

\n\u201cWe are delighted to receive this very productive feedback about Deltacel\u2122\/KB-GDT from the FDA, confirming our development strategy for this therapeutic candidate,\u201d stated Pietro Bersani, Chief Executive Officer of Kiromic. \u201cIt was a strategic decision to focus on metastatic stage 4 lung cancer as our first indication in addressing solid malignancies, and we are very heartened to be continuing to fulfill our mission to address solid malignancies, which represent more than 90% of all cancers.\u201d\n<\/p>\n

\nFurther reiterating Management\u2019s focus on executing the Deltacel-aligned development strategy, the Company has streamlined its operations and aligned key resources to advance its Deltacel\u2122 product candidate while maintaining its other product candidates Procel\u2122 and Isocel\u2122. As part of that aligned strategy and following a thorough evaluation to maximize operational efficiencies, Kiromic\u2019s management made the difficult yet necessary decision to eliminate 20 positions or approximately 29% of its workforce. The Company believes these key actions and overall strategy align with financing options it is actively pursuing.\n<\/p>\n

\n\u201cDeltacel\u2122 is our most advanced therapeutic candidate, and its use of allogeneic, non-viral, non-engineered off-the-shelf Gamma Delta T-cells (GDT) is a next-generation solution for patients. As such, this prioritization also mitigates supply-chain challenges associated with a virus-based approach. We believe these advantages will allow us to efficiently establish the platform\u2019s safety and tolerability and build upon Deltacel\u2122\u2019s previously demonstrated preclinical efficacy across multiple indications. With the FDA guidance in hand, we believe we\u2019ve further strengthened our case to align operations with Deltacel\u2122 and deliver value sooner to our shareholders,\u201d commented Bersani.\n<\/p>\n

About Kiromic BioPharma<\/b><\/p>\n

\nKiromic BioPharma, Inc. is a clinical-stage, fully integrated biotherapeutics company using its proprietary DIAMOND\u00ae<\/sup> artificial intelligence (AI) 2.0 platform to discover and develop celland gene therapies with a therapeutic focus on immuno-oncology and other diseases. Kiromic is developing a multi-indication allogeneic cell therapy platform that exploits the natural potency of Gamma Delta T-cells to target solid cancers. From its heritage as a cancer vaccine development company, Kiromic is focused on discovering, developing, and commercializing novel immuno-oncology applications through its robust product pipeline. The pipeline development is leveraged through the Company\u2019s proprietary target discovery engine called \u201cDIAMOND.\u201d Kiromic\u2019s DIAMOND is where data science meets target identification to dramatically compress the years and hundreds of millions of dollars required to develop a live drug. The Company maintains offices in Houston, Texas. To learn more, visit www.kiromic.com<\/a> and connect with us on Twitter and LinkedIn.\n<\/p>\n

Forward-Looking Statements<\/b><\/p>\n

\nThis press release contains forward-looking statements that involve substantial risks and uncertainties. Kiromic makes such forward-looking statements pursuant to the safe harbor provisions of the United States Private Securities Litigation Reform Act, Section 21E of the Securities Exchange Act of 1934, as amended, and other federal securities laws. All statements other than statements of historical facts are forward-looking statements. In some cases, you can identify forward-looking statements by terms such as: \u201cwill,\u201d \u201cpotential,\u201d \u201ccould,\u201d \u201ccan,\u201d \u201cbelieve,\u201d \u201cintends,\u201d \u201ccontinue,\u201d \u201cplans,\u201d \u201cexpects,\u201d \u201canticipates,\u201d \u201cestimates,\u201d \u201cmay,\u201d or the negative of these terms or other comparable terminology. These forward-looking statements include, but are not limited to, statements regarding: Kiromic\u2019s current and anticipated IND applications including statements regarding the scope of and timing for submission of an IND application; the Deltacel\u2122 product platform; the timing for submitting and activating Kiromic\u2019s IND applications and clinical trials; Kiromic\u2019s ability to achieve its objectives; the timing for the initiation and successful completion of Kiromic\u2019s clinical trials of its product candidates; the potential of Kiromic\u2019s product candidates. These forward-looking statements involve known and unknown risks, uncertainties and other factors that may cause actual results, levels of activity, performance, or achievements to be materially different from the information expressed or implied expressed or implied by these forward-looking statements. These risks and uncertainties include, but are not limited to, the risks and uncertainties discussed in our Annual Report on Form 10-K for the year ended December 31, 2021, and as detailed from time to time in our other SEC filings. You should not rely upon forward-looking statements as predictions of future events. Although we believe that the expectations reflected in the forward-looking statements are reasonable, we cannot guarantee that the future results, levels of activity, performance, or events and circumstances reflected in the forward-looking statements will be achieved or occur. Moreover, neither we nor any other person assumes responsibility for the accuracy and completeness of the forward-looking statements. Such forward-looking statements relate only to events as of the date of this press release. We undertake no obligation to update any forward-looking statements except to the extent required by law.\n<\/p>\n

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View source version on businesswire.com: <\/span>https:\/\/www.businesswire.com\/news\/home\/20221006005406\/en\/<\/a><\/span><\/p>\n

Kiromic BioPharma
\n<\/b>
Linda Phelan Dyson, MPH
\n
Global Head, Corporate Communications
\n
ldyson@kiromic.com
\n<\/a>
M: 281-468-7683\n<\/p>\n

LHA Investor Relations
\n<\/b>
Tirth T. Patel
\n
tpatel@lhai.com
\n<\/a>
212-201-6614\n<\/p>\n

KEYWORDS:<\/b> United States North America Texas<\/p>\n

INDUSTRY KEYWORDS:<\/b> Health Technology Biometrics Clinical Trials Artificial Intelligence Pharmaceutical<\/p>\n

MEDIA:<\/b><\/p>\n\n\n\n\n
Logo<\/b><\/font><\/td>\n<\/tr>\n
\"Logo\"<\/td>\n<\/tr>\n
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Kiromic BioPharma Announces FDA Feedback from Type B Pre-IND Meeting Confirms Deltacel Development Strategy Company Reiterates Deltacel is Next Clinical Trial Candidate, with Projected Clinical Trial Launch Expected in Q1 2023 Company is Streamlining Operations to Execute Deltacel-Aligned Development Strategy HOUSTON–(BUSINESS WIRE)–Kiromic BioPharma, Inc. (NASDAQ: KRBP) (\u201cKiromic\u201d or the \u201cCompany\u201d), a clinical-stage fully-integrated biotherapeutics company using its proprietary DIAMOND\u00ae artificial intelligence and data mining platform to develop cell and gene therapies with a focus on immuno-oncology, announces it received validating written feedback on October 4, 2022 from the FDA pursuant to its Type B Pre-IND meeting request regarding its Deltacel\u2122 development strategy. The purpose of the Pre-IND meeting request was to seek alignment with and to obtain FDA guidance on … <\/p>\n

Continue reading “Kiromic BioPharma Announces FDA Feedback from Type B Pre-IND Meeting Confirms Deltacel Development Strategy”<\/span><\/a><\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[],"tags":[],"class_list":["post-692896","post","type-post","status-publish","format-standard","hentry"],"yoast_head":"\nKiromic BioPharma Announces FDA Feedback from Type B Pre-IND Meeting Confirms Deltacel Development Strategy - Market Newsdesk<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.marketnewsdesk.com\/index.php\/kiromic-biopharma-announces-fda-feedback-from-type-b-pre-ind-meeting-confirms-deltacel-development-strategy\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Kiromic BioPharma Announces FDA Feedback from Type B Pre-IND Meeting Confirms Deltacel Development Strategy - Market Newsdesk\" \/>\n<meta property=\"og:description\" content=\"Kiromic BioPharma Announces FDA Feedback from Type B Pre-IND Meeting Confirms Deltacel Development Strategy Company Reiterates Deltacel is Next Clinical Trial Candidate, with Projected Clinical Trial Launch Expected in Q1 2023 Company is Streamlining Operations to Execute Deltacel-Aligned Development Strategy HOUSTON–(BUSINESS WIRE)–Kiromic BioPharma, Inc. (NASDAQ: KRBP) (\u201cKiromic\u201d or the \u201cCompany\u201d), a clinical-stage fully-integrated biotherapeutics company using its proprietary DIAMOND\u00ae artificial intelligence and data mining platform to develop cell and gene therapies with a focus on immuno-oncology, announces it received validating written feedback on October 4, 2022 from the FDA pursuant to its Type B Pre-IND meeting request regarding its Deltacel\u2122 development strategy. 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(NASDAQ: KRBP) (\u201cKiromic\u201d or the \u201cCompany\u201d), a clinical-stage fully-integrated biotherapeutics company using its proprietary DIAMOND\u00ae artificial intelligence and data mining platform to develop cell and gene therapies with a focus on immuno-oncology, announces it received validating written feedback on October 4, 2022 from the FDA pursuant to its Type B Pre-IND meeting request regarding its Deltacel\u2122 development strategy. 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