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Ceapro Inc V.CZO

Ceapro Inc. is a Canada-based biotechnology company. The Company is involved in the development of extraction technology and the application of this technology to the production of extracts and active ingredients from oats and other renewable plant resources. Its primary business activities relate to the development and commercialization of natural products for personal care, cosmetic, human, and animal health industries using technology, natural, renewable resources, and developing products, technologies, and delivery systems. The Company's products include a commercial line of natural active ingredients, including beta glucan, avenanthramides (colloidal oat extract), oat powder, oat oil, oat peptides, and lupin peptides, a commercial line of natural anti-aging skincare products, utilizing active ingredients, including beta glucan and avenanthramides and veterinary therapeutic products, including an oat shampoo, an ear cleanser, and a dermal complex/conditioner.


TSXV:CZO - Post by User

Comment by prophetoffactzon Mar 03, 2024 9:32am
44 Views
Post# 35911863

RE:RE:RE: Bottom line on the merger

RE:RE:RE: Bottom line on the mergerCiao, "the Macrilen story is old and tired..."

AEZS's diagnostic test has never been approved for the key childhood market. The pediatric clinical trial was expected to be fully enrolled by the end of 2023 after delays due to COVID and Putin's invasion of Ukraine. Some of the trial had been planned for Russia. The data and a deal are about to hit the market and Gilles is well positioned inside of AEZS to understand what is coming. It's like having inside information. 
The market isn't as well positioned to know what's coming. Pediatric approval will allow a full-scale marketing effort accross all populations for the first time and help drive awareness in adults. The market is aware of the need for growth hormone deficiency testing in children due to the health implications but suffers from a lack of awareness in the adult population. For adults growth hormone deficiency can result in changes in body composition, muscle tone, carsiovascular parameters, quality of life and mortality. H.C. Wainwright has a US$15 targer price for AEZS likely driven substantially by the test. AEZS's pediatric clinical trial is also set up as a potential standalone test. Currently two tests are generally used to diagnose growth hormone deficiency. Who will want the cost and burden of running a second test? Managing a child can be burdensome enough with one test. Eliminating a second test, and making its needlesticks, and side-effects unnecessary would be a significant benefit. AEZS's test also results in less over-diagnosis. The contra-indications for an insulin tolerance test in the adult population are also significant.   


Abstract

Purpose: The diagnosis of adult GH deficiency (AGHD) is challenging and often requires confirmation with a GH stimulation test (GHST). The insulin tolerance test (ITT) is considered the reference standard GHST but is labor intensive, can cause severe hypoglycemia, and is contraindicated for certain patients. Macimorelin, an orally active GH secretagogue, could be used to diagnose AGHD by measuring stimulated GH levels after an oral dose.

Materials and methods: The present multicenter, open-label, randomized, two-way crossover trial was designed to validate the efficacy and safety of single-dose oral macimorelin for AGHD diagnosis compared with the ITT. Subjects with high (n = 38), intermediate (n = 37), and low (n = 39) likelihood for AGHD and healthy, matched controls (n = 25) were included in the efficacy analysis.

Results: After the first test, 99% of macimorelin tests and 82% of ITTs were evaluable. Using GH cutoff levels of 2.8 ng/mL for macimorelin and 5.1 ng/mL for ITTs, the negative agreement was 95.38% (95% CI, 87% to 99%), the positive agreement was 74.32% (95% CI, 63% to 84%), sensitivity was 87%, and specificity was 96%. On retesting, the reproducibility was 97% for macimorelin (n = 33). In post hoc analyses, a GH cutoff of 5.1 ng/mL for both tests resulted in 94% (95% CI, 85% to 98%) negative agreement, 82% (95% CI, 72% to 90%) positive agreement, 92% sensitivity, and 96% specificity. No serious adverse events were reported for macimorelin.

Conclusions: Oral macimorelin is a simple, well-tolerated, reproducible, and safe diagnostic test for AGHD with accuracy comparable to that of the ITT. A GH cutoff of 5.1 ng/mL for the macimorelin test provides an excellent balance between sensitivity and specificity.


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