Thursday, April 26, 2018

Antibe Therapeutics Announces CEO Letter to Shareholders


Antibe Therapeutics Inc. (TSXV: ATE, OTCQB: ATBPF):


To our stakeholders,


The recent success of our lead drug, ATB-346, in its Phase 2B
gastrointestinal (“GI”) safety clinical study was a significant
milestone for Antibe and represented a major inflection point in our
value. Furthermore, we are now one clinical study away from the
strategic monetization of our drug platform for the major markets. With
such an important and exciting time ahead of us, we thought this would
be an ideal opportunity to communicate our strategy for the next year
and beyond.


Nearly ten years ago, Antibe was formed to develop safer medicines for
pain and inflammation by leveraging our novel hydrogen sulfide (“H2S”)
technology. Over this period, our strategy to maximize value for
shareholders has remained consistent: advance our drug candidates to
Phase 2 proof-of-concept data and secure high-value partnerships for the
large pharmaceutical markets. Fast forward to 2018: we now have
unequivocal validation of our H2S platform, and are
well-positioned to conclude a series of transformational partnerships
over the next 12-18 months.


This progress could not have been done without the support of our
shareholders, who are now being rewarded for their patience over the
years. In the months ahead, our team will be working diligently to
ensure that our clinical and business development activities are well
aligned with our strategy to maximize shareholder return.


Recent Phase 2B Study Confirms Best-in-Class Status for Drug
Platform


In Antibe’s latest Phase 2B study, ATB-346 showed unequivocal
superiority to naproxen in GI safety (2.5% versus 42.1% ulceration rate)
in 244 healthy volunteers. This human proof-of-concept data replicated
the results of our pre-clinical studies, and provides clear validation
of the GI-protective properties of our H2S technology. The
full analysis of this study will be reported this quarter. We are now
pushing forward with the planned Phase 2 effectiveness study for
ATB-346, and are accelerating development of our other H2S
platform drugs. Each of Antibe’s drugs has blockbuster potential, and
would provide physicians and consumers with radically safer alternatives
to today’s NSAIDs and to the multi-dimensional dangers of
corticosteroids and opiates.


Upcoming Phase 2 Effectiveness Study Designed to Validate Efficacy
of ATB-346


With human GI safety for ATB-346 now firmly established, our next
clinical objective is to validate its effectiveness at reducing pain in
osteoarthritis (“OA”) patients. In August 2016, Antibe released top-line
data from a Phase 2A study that showed considerable pain relief for
ATB-346 at a once-daily dose of 250 mg – the pain relief observed was
nearly double that of naproxen and Celebrex based on published data.
Although these results were encouraging, the study was conducted in a
small number of patients and was not controlled. Our upcoming Phase 2
effectiveness study is designed to validate the pain reduction efficacy
of ATB-346 (versus control) and will be conducted in approximately 250
OA patients. In addition, we have biomarker data derived from Phase 1
and Phase 2 blood assays that suggest ATB-346 is effective at lower
doses; for this reason, the study will include two additional dosing
cohorts with the goal of determining the lowest effective dose.
Preparations are well underway for this study and we anticipate
commencing it by July with a data read-out in Q4 2018.


Additional Clinical Activities to Support Global Partnering Efforts


In addition to the Phase 2 effectiveness study, Antibe will also be
strategically allocating R&D spend towards activities that we feel will
be of the most value to global partners. These activities include: (i)
long-range animal toxicology studies (6 months and 9 months) for
ATB-346, a standard regulatory requirement for approval of any drug;
(ii) additional metabolic studies for ATB-346 to further strengthen our
understanding of its pharmacokinetic profile; and (iii) the completion
of IND-enabling studies for both ATB-352 and ATB-340, Antibe’s two other
H2S platform drugs. Although ATB-352 and ATB-340 are earlier
stage, both individually represent blockbuster drug opportunities and
have been considerably de-risked by the latest validation of our H2S
technology. We remain particularly excited about the potential of
ATB-352, a non-addictive, potent analgesic for acute pain that directly
addresses the global opioid epidemic, a crisis that the world is
struggling to contain.


Partnering Discussions Building Momentum


In the past, Antibe’s partnering efforts were focused on strategically
out-licensing the rights for smaller markets (i.e., outside of the
United States and Western Europe). We continue to have these discussions
and have been successful in concluding two regional deals to-date – this
activity remains valuable as it provides non-dilutive funding and
further validation of our drug platform. The recent human
proof-of-concept GI safety data have undoubtedly benefited these
on-going discussions, and more importantly, now allow us to engage
multinational pharmaceutical firms to secure strategic partnerships for
the large markets. As mentioned earlier, our clinical development
activities in the next 12 months are designed to maximize the value of
our drug platform and strengthen our position as we engage potential
partners.


Commercial Asset in Regenerative Medicine Well-Positioned For
Growth


Our subsidiary, Citagenix Inc. (“Citagenix”), is nearly done assembling
the building blocks for its growth strategy in the dental regenerative
medicine market. Citagenix’s sales team in the United States is working
hard at expanding its distribution network, and recently signed Benco
Dental, the 3rd largest dental distributor in the US by
market share. Antibe’s relationship with Citagenix has been a symbiotic
one: Antibe provided the resources to position Citagenix on a growth
trajectory while Citagenix provided valuable diversification. With
Citagenix now on a path to growth and Antibe’s drug development
activities de-risked considerably by the recent GI safety data, our team
will now begin exploring strategic alternatives for Citagenix in an
effort to unlock value for shareholders.


Strong Balance Sheet and Maturing Capital Markets Strategy


Antibe’s balance sheet is well-funded with approximately $5 million of
cash, and recently benefited from the entire conversion of its
debentures. The upcoming Phase 2 effectiveness trial for ATB-346 will be
funded entirely with cash-on-hand. In addition, given our stage of
development, we are now exploring a listing on the NASDAQ exchange to
grow our institutional investor base in the United States.


We look forward to the year ahead as we drive closer towards our goal of
bringing safer medicines to market for pain and inflammation.


Sincerely,


Dan Legault
Chief Executive Officer


About Antibe Therapeutics Inc.


Antibe develops safer medicines for pain and inflammation. Antibe’s
technology involves linking a hydrogen sulfide-releasing molecule to an
existing drug to produce a patented, improved medicine. Antibe’s lead
drug ATB-346 targets the global need for a safer, non-addictive drug for
chronic pain and inflammation. ATB-352, the second drug in Antibe’s
pipeline, targets the urgent global need for a non-addictive analgesic
for treating severe acute pain, while ATB-340 is a GI-safe derivative of
aspirin. https://ift.tt/2BWXRQt;


Antibe’s subsidiary, Citagenix Inc. (“Citagenix”), is a leader in the
sales and marketing of tissue regenerative products servicing the
orthopedic and dental marketplaces. Since its inception in 1997,
Citagenix has become an important source of knowledge and experience for
bone regeneration in the Canadian medical device industry. Citagenix is
active in 15 countries, operating in Canada through its direct sales
teams, and internationally via a network of distributor partnerships. www.citagenix.com.


Forward Looking Information


This news release includes certain forward-looking statements, which may
include, but are not limited to, the proposed licensing and development
of drugs and medical devices. Any statements contained herein that are
not statements of historical facts may be deemed to be forward-looking,
including those identified by the expressions “will”, “anticipate”,
“believe”, “plan”, “estimate”, “expect”, “intend”, “propose” and similar
expressions. Forward-looking statements involve known and unknown risks
and uncertainties that could cause actual results, performance, or
achievements to differ materially from those expressed or implied in
this news release. Factors that could cause actual results to differ
materially from those anticipated in this news release include, but are
not limited to, the Company’s inability to secure additional financing
and licensing arrangements on reasonable terms, or at all, its inability
to execute its business strategy and successfully compete in the market,
and risks associated with drug and medical device development generally.
Antibe Therapeutics Inc. assumes no obligation to update the
forward-looking statements or to update the reasons why actual results
could differ from those reflected in the forward-looking statements
except as required by applicable law.



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Full steam ahead for Dunkirk pharmaceutical plant

Data Integrity Code of Conduct

Data is the great enabler when it comes to manufacturing processes. But not all data is good. Industry pundits estimate that about 85 percent of the data generated in manufacturing has absolutely no value at all. Which makes one wonder if some of that useless information can cause problems.

What to do with all that data—the good and the bad— is not a new area of discussion, but it is still on the forefront of the minds of pharmaceutical executives, especially as they respond to Food & Drug Administration (FDA) enforcement actions. In recent years, there has been an increase in warning letters to companies around deviations from current good manufacturing practices (CGMP) in manufacturing facilities.

The number of drug GMP warning letters went from 42 in 2015 to 102 in 2016 to 114 in 2017. This puts more emphasis on data integrity in the industry.

The FDA uses the acronym ALCOA to define data integrity, meaning, it is attributable (who did it/source data), legible (recorded in a permanent medium and it is readable), contemporaneous (data recorded in real time), original (an original or certified true copy of data), and accurate (no errors or editing performed without documented amendments).

Addressing ALCOA took center stage during the recent Interphex conference in New York. A keynote presentation by Els Poff, executive director of the data integrity center of excellence at Merck, discussed details of data integrity from log-ins to definitions to validation and verification—as it relates to ALCOA. In addition, Poff, who is on the Parenteral Drug Association (PDA) data integrity task force, said the organization is working on a comprehensive set of tools for industry that includes a technical report, which will be available at the end of the year, that will address new requirement challenges related to Industry 4.0 and Big Data.

The PDA has already released the Elements of a Code of Conduct for Data Integrity, which addresses the culture of data integrity. It touches on actions that can contaminate data, like employee errors or system configuration problem with electronic data handling.

This code of conduct is important because, like cybersecurity, data integrity is everyone’s business. The document provides an in-depth guidance for life science companies with a focus around a handful of actions :

  • Applicability – The company should establish requirements and implement programs to provide employees with training on the fundamental principles of data integrity.
  • Data collection, analysis, reporting and retention – The company shall establish procedures, documentation and control systems to maintain data integrity by collecting, analyzing and reporting data on paper and in computer systems with the appropriate security, audit trails, validation and oversight of electronic documents.
  • Electronic access security measures – Any computer data acquisition system should have secure access to prevent unauthorized changes to electronic data.
  • Investigating wrongful acts – Procedures for investigating an alleged falsification shall include documented in-depth review, conducted in a fair and balanced manner by independent personnel.
  • Data integrity of outsourced services and purchased raw materials – as part of a vendor/supplier qualification program, the company will confirm that contractors, vendors or other third party providers have established policies, standards, procedures or other documents that adhere to data integrity requirements.

The PDA code of conduct boils down to having a common understanding of the expectations for employee and management behaviors. Moreover, the path to data integrity should be “complete, consistent and enduring,” Merck’s Poff noted in her keynote. “Do you have all of the data and meta data over the lifecycle? Do you have processes in place with data and time stamps? Is the data on media that is still retrievable?”

This is not rocket science. But we are living in the era of organization. And, many of these things can get overlooked. To get your pharma house in order, download the free PDA code of conduct document.

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Tuesday, April 24, 2018

2 Day Course: The A to Z’s of Microbial Control, Monitoring and Validation of Water Systems (San Francisco, CA – August 23-24, 2018) – ResearchAndMarkets.com

DUBLIN–(BUSINESS WIRE)–The “The
A to Z’s of Microbial Control, Monitoring and Validation of Water
Systems for Pharmaceuticals, Biologics, Medical Devices, Cosmetics, and
Personal Care Products”
conference has been added to ResearchAndMarkets.com’s
offering.

This course is designed to provide a microbiology-focused education
about all aspects of water systems and how biofilm manages to thrive
there.

Prior microbiological education or training, though a plus, is not a
requirement, since this training is for everyone involved with water
systems, from the lab to utility room operations. The instructor will
provide the necessary background needed to understand this very
important subject matter.

This understanding is essential for the proper design, validation,
operation, monitoring, and maintenance of a high purity water system.
Without this understanding, water system control and monitoring consists
of a set of rules that often don’t work or result in erroneous
monitoring data and can cause everything from very costly and
unnecessary system downtime to patient injury and product recalls.

Agenda

Day 1 (8:30 AM – 4:30 PM)

  • Basics of Water System Biofilm Control by Design & Operation
  • Successful Water System Sanitization
  • Common Sense Water System Validation
  • Understanding and Controlling Endotoxin
  • Harmonizing vs. Optimizing Water Microbial Testing for System Quality
    Control

Day 2 (8:30 AM – 4:30 PM)

  • Microbial Enumeration Issues with High Purity Water Systems
  • Reducing Water Microbial Excursions & Improving Investigations
  • Water System Investigation “How-To’s” and Example Case Studies
  • Leadership in MFG Contamination Control: The Microbiology Lab
  • USP Chapter: What USP Says about PW, WFI, Pure Steam & Micro Issues
  • Guarding Against Common Pharmaceutical Water System Inspection Pitfalls

For more information about this conference visit https://ift.tt/2FdWvyu

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Tetra Bio-Pharma Signs Landmark Commercialization Term Sheet for its Lead Pharmaceutical Product, PPP001, in Israel

OTTAWA, ONTARIO–(Marketwired – April 24, 2018) – Tetra Bio-Pharma Inc. (“Tetra” or the “Company”) (TSX VENTURE:TBP) (OTCQB:TBPMF), announced today that the Company has signed a first binding term sheet for the marketing and distribution of PPP001 in Israel with Kamada Ltd., a leading pharmaceutical company. The signing of a Definitive Distribution Agreement is expected to follow shortly. PPP001 is being developed to be the first smokable cannabis product for advanced cancer pain available under prescription.

This first international market commercialization agreement represents a significant milestone and a validation of Tetra Bio-Pharma’s business model with a leading Israel-based pharmaceutical company. Israel, like Canada, is considered one of the world leaders in the production and development of cannabinoid-based products. Kamada is a company with two FDA-approved products and an Israeli-based distribution segment that has demonstrated continued growth. Tetra Bio-Pharma intends to work closely with Kamada as PPP001 advances towards regulatory approval and commercial launch in Israel.

Under the terms of the anticipated final agreement, Kamada will be responsible for registering the product, as well as all marketing and distribution, in Israel. Tetra will be eligible to receive certain milestone payments and an undisclosed percentage of the sales of PPP001 generated by Kamada in Israel.

About PPP001

On April 4, 2018, Tetra Bio-Pharma officially started the Phase 3 trial for PPP001 indicated for terminal stage cancer patients with a goal to improving the quality of life of these patients as well as minimizing their pain. PPP001 is being developed to be the first smokable cannabis product for advanced cancer pain available under prescription.

About Tetra Bio-Pharma: Tetra Bio-Pharma (TSX VENTURE:TBP) (OTCQB:TBPMF) is a biopharmaceutical leader in cannabinoid-based drug discovery and clinical development. Tetra is focusing on three core business pillars: clinical research, pharmaceutical promotion and retail commercialization of cannabinoid-based products. Tetra Bio-Pharma is currently developing a pipeline of five cannabinoid-based products using different delivery systems such as smokable pellets, oral tablets, eye drops and topical ointments. More information at: www.tetrabiopharma.com

Source: Tetra Bio-Pharma

Neither the TSX Venture Exchange nor its Regulation Services Provider (as that term is defined in the policies of the TSX Venture Exchange) accepts responsibility for the adequacy or accuracy of this release.

Forward-looking statements

Some statements in this release may contain forward-looking information. All statements, other than of historical fact, that address activities, events or developments that the Company believes, expects or anticipates will or may occur in the future (including, without limitation, statements regarding potential acquisitions and financings) are forward-looking statements. Forward-looking statements are generally identifiable by use of the words “may”, “will”, “should”, “continue”, “expect”, “anticipate”, “estimate”, “believe”, “intend”, “plan” or “project” or the negative of these words or other variations on these words or comparable terminology. Forward-looking statements are subject to a number of risks and uncertainties, many of which are beyond the Company’s ability to control or predict, that may cause the actual results of the Company to differ materially from those discussed in the forward-looking statements. Factors that could cause actual results or events to differ materially from current expectations include, among other things, without limitation, the inability of the Company, through its wholly-owned subsidiary, GrowPros MMP Inc., to obtain a license for the production of medical marijuana; failure to obtain sufficient financing to execute the Company’s business plan; competition; regulation and anticipated and unanticipated costs and delays, the success of the Company’s research strategies, the applicability of the discoveries made therein, the successful and timely completion and uncertainties related to the regulatory process, the timing of clinical trials, the timing and outcomes of regulatory or intellectual property decisions and other risks disclosed in the Company’s public disclosure record on file with the relevant securities regulatory authorities. Although the Company has attempted to identify important factors that could cause actual results or events to differ materially from those described in forward-looking statements, there may be other factors that cause results or events not to be as anticipated, estimated or intended. Readers should not place undue reliance on forward-looking statements. While no definitive documentation has yet been signed by the parties and there is no certainty that such documentation will be signed The forward-looking statements included in this news release are made as of the date of this news release and the Company does not undertake an obligation to publicly update such forward-looking statements to reflect new information, subsequent events or otherwise unless required by applicable securities legislation.

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