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ImmuCell Announces Submission of CMC Technical Section to the FDA

Key Takeaway: ImmuCell Corporation (NASDAQ: ICCC) announced the submission of the Chemistry, Manufacturing and Controls (CMC) Technical Section for its product Re-Tain® to the FDA. This submission, which took place on August 18, 2023, follows the company's prior announcement of a planned timeline. The FDA review process is anticipated to take six months, during which the company expressed optimism about future opportunities related to this product. Re-Tain® is designed to treat subclinical mastitis in dairy cows without the need for milk discard, positioning itself as an alternative to traditional antibiotics.

Market Sentiment Analysis

POSITIVE FACTORS

  • Successful submission of the CMC Technical Section for Re-Tain® to the FDA.
  • Achievement aligns with previously stated objectives and timelines.
  • Opportunity ahead as the submission enters a review process with the FDA.

Full Press Release Details

PORTLAND, Maine, Aug. 29, 2023 (GLOBE NEWSWIRE) -- ImmuCell Corporation (Nasdaq: ICCC) (“ImmuCell” or the “Company”), a growing animal health company that develops, manufactures and markets scientifically proven and practical products that improve the health and productivity of dairy and beef cattle, announced today that it recently submitted the Chemistry, Manufacturing and Controls (CMC) Technical Section for Re-Tain® to the FDA.
On August 10, 2023, the Company issued a disclosure stating that it anticipated making this submission “shortly” after the filing of its Quarterly Report on Form 10-Q. The Company is now confirming that this objective was achieved.
“For the benefit of clarity, we want to inform investors that this important step in the regulatory process was taken on August 18, 2023,” commented Michael F. Brigham, President and CEO of ImmuCell. “This kind of submission is subject to a six-month review by the FDA, and we are excited about the opportunity ahead.”
ImmuCell Corporation's (Nasdaq: ICCC) purpose is to create scientifically proven and practical products that improve the health and productivity of dairy and beef cattle. ImmuCell manufactures and markets First Defense®, providing Immediate Immunity™ to newborn dairy and beef calves, and is in the late stages of developing Re-Tain®, a novel treatment for subclinical mastitis in dairy cows without a milk discard requirement that provides an alternative to traditional antibiotics. Press releases and other information about the Company are available at: http://www.immucell.com.
Contacts: Michael F. Brigham, President and CEO
ImmuCell Corporation
(207) 878-2770
Joe Diaz, Robert Blum and Joe Dorame
Lytham Partners, LLC
(602) 889-9700
iccc@lythampartners.com
Cautionary Note Regarding Forward-Looking Statements (Safe Harbor Statement):
This Press Release contains or may contain “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995, as amended. Forward-looking statements can be identified by the fact that they do not relate strictly to historical or current facts and will often include words such as “expects”, “may”, “anticipates”, “aims”, “intends”, “would”, “could”, “should”, “will”, “plans”, “believes”, “estimates”, “targets”, “projects”, “forecasts”, “seeks” and similar words and expressions. Such statements include, but are not limited to, any forward-looking statements relating to: our plans and strategies for our business; projections of future financial or operational performance; the scope and timing of ongoing and future product development work and commercialization of our products; the timing and completeness of any regulatory submissions or milestones and possible regulatory approval of any of our products (including Re-Tain®) and any other statements that are not historical facts. These statements are intended to provide management's current expectation of future events as of the date of this Press Release, are based on management's estimates, projections, beliefs and assumptions as of the date hereof; and are not guarantees of future performance. Such statements involve known and unknown risks and uncertainties that may cause the Company's actual results, financial or operational performance or achievements to be materially different from those expressed or implied by these forward-looking statements, including, but not limited to, those risks and uncertainties detailed from time to time in filings we make with the Securities and Exchange Commission (SEC), including our Quarterly Reports on Form 10-Q, our Annual Reports on Form 10-K and our Current Reports on Form 8-K. In addition, there can be no assurance that future risks, uncertainties or developments affecting us will be those that we anticipate. We undertake no obligation to update any forward-looking statement, whether written or oral, that may be made from time to time, whether as a result of new information, future developments or otherwise.

Frequently Asked Questions

What recent submission did ImmuCell make to the FDA?

ImmuCell submitted the Chemistry, Manufacturing and Controls Technical Section for Re-Tain®.

When was the CMC submission made to the FDA?

The CMC submission was made on August 18, 2023.

What does Re-Tain® treat in dairy cows?

Re-Tain® is a novel treatment for subclinical mastitis in dairy cows.

What key product does ImmuCell offer for calves?

ImmuCell offers First Defense®, which provides Immediate Immunity™ to calves.

How long is the FDA's review period for the submission?

The FDA review period for the submission is six months.

Last updated: Aug 29, 2023