Day: June 13, 2022

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Republic of South Africa Medical Marijuana Dispensaries Acquisitions LLC (RSAMMDA.LLC) Completes Acquisition of Protext Mobility, Inc. (TXTM)

JOHANNESBURG, South Africa, June 13, 2022 (GLOBE NEWSWIRE) — Republic of South Africa Medical Marijuana Dispensaries Acquisitions LLC (“RSAMMDA.LLC”) is pleased to announce it has closed on the acquisition of Protext Mobility, Inc (OTC PINK: TXTM) (A.K.A. Protext Pharma) in a share exchange whereby 100% of capital stock in RSAMMDA.LLC will be exchanged for Preferred Stock in Protext. RSAMMDA.LLC. is a jointly owned company focused on acquistions with two principals, Mr. Dylon Du Plooy and Dr. Ahmed Jamaloodeen (“Dr. J”) who represent the South African business entities of RSAMMD and Leeds Boerdery. RSAMMD is a South African pioneer in the research, cultivation, production and distribution of medical cannabis and cannabinoids. Leeds Boerdery, controlled by Dr. J, owns the 5000 Hectacre New Castle Farm as well as federally issued cannabis and hemp licenses issued by the Government of South Africa. RSAMMD management have taken over the daily operations of Protext headed by Mr. Du Plooy as CEO and Director, and Dr. Jamaloodeen as President and Chairman of the Board.

Mr. Dylon Du Plooy, Protext CEO and Principal of RSAMMD.LLC, commented, “This transaction has been a long time in the making. For the past couple years we have been focused on building our operations in South Africa and globally, where have built an extensive infrastructure and global cannabis/hemp business. During this period of time, we have invested heavily in building a significant cannabis/hemp operation to facilitate complete seed to sale, R&D, global off-take agreements for end product as well as all the extraction infrastructure needed to create what we believe to be some of the highest quality hemp and cannabis on the planet. In South Africa right now, we have just completed our semi-annual grow. RSAMMD in Joint Venture with Leeds Boerdery, cultivated hemp and cannabis crops this past season on a combined 1000+ hectacres. All of this is done under federally issued permits and licenses to grow, import/export hemp and cannabis, as well as research permits for conducting testing of final products for human consumption and medicinal benefits.”

Dr. Jamaloodeen, Protext President and Chairman, commented, “We are excited about this transaction and taking Protext to the next level. We believe there to be numerous synergies to incorporate the Protext proprietary live plant extraction technology and processes into our existing infrastructure. We envision adding other assets into the operations of Protext, including our off-take agreements and present sales, with the goal of uplifting exchanges in the future. As previously announced, Protext and RSAMMD jointly worked together and conducted a series of tests on live cannabis to prove out that the Kettle system and extraction technologies did what they were supposed to do. We look forward to discussing this further as well as our upcoming operational plans.”

“Over the coming days and weeks, we will be sharing our immediate term road map and long-term plans we are developing for Protext which should translate into increasing shareholder value. These plans include adding other valuable assets to the company which complement the core business, and executing on commercializing the proprietary live plant extraction technology as well as deploying our crypto platform, with a TXTM token which we are excited to rollout very soon,” concluded Mr. Du Plooy.

CONTACT INFORMATION
For all media inquiries or for further information, please contact
Dylon Du Plooy at: dylon@rsammd.co.za
Dr.J at: exportintl@aol.com

About RSAMMD
RSAMMD Acquisitions LLC is a jointly owned business of RSAMMD, a South African pioneer in the research, cultivation, production and distribution of medical cannabis and cannabinoids, and Dr. J, who operates the 5000 Hectacre New Castle Farm as well as the federally issued cannabis and hemp licenses. Together, we partner with leading hospitals and universities globally to advance the clinical benefits and applications of cannabinoids.

RSAMMD’s founders are a group of medical doctors and pharmacists, and cannabis activists who have been at the forefront of medical cannabis legislation and South African cannabis legalization, which took place in September 2018. We are committed to the advancement of technology and scientific research that leads to an improved quality of life for patients around the world.
Please visit www.rsammd.co.za for further information.

About Protext (OTC PINK: TXTM)
Through previously disclosed acquisitions, Protext has engaged in the research, testing and commercialization of highly bioavailable botanical products all-natural ingredients formulated for nutraceutical and pharmaceutical applications through the use of proprietary live plant extraction technology.

Safe Harbor Statement
This release contains forward-looking statements that are based upon current expectations or beliefs, as well as a number of assumptions about future events. Although we believe that the expectations reflected in the forward-looking statements and the assumptions upon which they are based are reasonable, we can give no assurance or guarantee that such expectations and assumptions will prove to have been correct. Forward-looking statements are generally identifiable by the use of words like “may,” “will,” “should,” “could,” “expect,” “anticipate,” “estimate,” “believe,” “intend,” or “project” or the negative of these words or other variations on these words or comparable terminology. The reader is cautioned not to put undue reliance on these forward-looking statements, as these statements are subject to numerous factors and uncertainties, including but not limited to: adverse economic conditions, competition, adverse federal, state and local government regulation, international governmental regulation, inadequate capital, inability to carry out research, development and commercialization plans, loss or retirement of key executives and other specific risks. To the extent that statements in this press release are not strictly historical, including statements as to revenue projections, business strategy, outlook, objectives, future milestones, plans, intentions, goals, future financial conditions, events conditioned on stockholder or other approval, or otherwise as to future events, such statements are forward-looking, and are made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. The forward-looking statements contained in this release are subject to certain risks and uncertainties that could cause actual results to differ materially from the statements made. The company disclaims any obligation to update information contained in any forward-looking statement. This press release shall not be deemed a general solicitation.

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Philips to repurchase up to 3.2 million shares to cover long-term incentive and employee stock purchase plans

June 13, 2022

Amsterdam, the Netherlands – Royal Philips (NYSE: PHG, AEX: PHIA) today announced that it will repurchase up to 3.2 million shares to cover certain of its obligations arising from its long-term incentive and employee stock purchase plans. At the current share price, the shares represent an amount of up to approximately EUR 68 million.

The repurchases will be executed through one or more individual forward transactions, expected to be entered into in the second and/or the third quarter of 2022, in accordance with the Market Abuse Regulation and within the limits of the authorization granted by the company’s General Meeting of Shareholders on May 10, 2022. Philips expects to take delivery of the shares in 2024. Further details will be available via this link.

For further information, please contact:

Ben Zwirs
Philips Global Press Office
Tel.: +31 6 1521 3446
E-mail: ben.zwirs@philips.com

Derya Guzel
Philips Investor Relations
Tel.: +31 20 59 77055
E-mail: derya.guzel@philips.com

About Royal Philips
Royal Philips (NYSE: PHG, AEX: PHIA) is a leading health technology company focused on improving people’s health and well-being, and enabling better outcomes across the health continuum – from healthy living and prevention, to diagnosis, treatment and home care. Philips leverages advanced technology and deep clinical and consumer insights to deliver integrated solutions. Headquartered in the Netherlands, the company is a leader in diagnostic imaging, image-guided therapy, patient monitoring and health informatics, as well as in consumer health and home care. Philips generated 2021 sales of EUR 17.2 billion and employs approximately 79,000 employees with sales and services in more than 100 countries. News about Philips can be found at www.philips.com/newscenter.

Forward-looking statements
This release contains certain forward-looking statements with respect to the financial condition, results of operations and business of Philips and certain of the plans and objectives of Philips with respect to these items. Examples of forward-looking statements include statements made about the strategy, estimates of sales growth, future EBITA, future developments in Philips’ organic business and the completion of acquisitions and divestments. By their nature, these statements involve risk and uncertainty because they relate to future events and circumstances and there are many factors that could cause actual results and developments to differ materially from those expressed or implied by these statements.

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Philips announces positive three-year clinical research results from its Tack Optimized Balloon Angioplasty (TOBA) II below-the-knee (BTK) clinical trial

June 13, 2022

  • For below-the-knee arterial dissection repair following balloon angioplasty, innovative medical technology shows sustained treatment effect and positive impact on quality of life for patients with critical limb ischemia (CLI)
  • First and only FDA-approved device of its kind demonstrates consistently high rates of target limb salvage (93.9%) and freedom from clinically-driven target lesion revascularization (69.6%)

Amsterdam, the Netherlands – Royal Philips (NYSE: PHG, AEX: PHIA), a global leader in health technology, today announced the latest results from the Tack Optimized Balloon Angioplasty (TOBA) II below-the-knee (BTK) clinical trial, demonstrating that the Philips endovascular system – Tack (4F) – the first and only device of its kind approved by the U.S. Food and Drug Administration (FDA), provides a sustained treatment effect and positive impact on quality of life for patients with critical limb ischemia (CLI), a severe stage of peripheral arterial disease (PAD), out to three years of clinical follow-up.

CLI occurs when an obstruction in an artery severely reduces blood flow, causing painful wounds, debilitating rest pain, recurring ulcers and life-threatening infection. If left untreated, 50% of patients with CLI will undergo an amputation or die within the first year [1].

The TOBA II BTK trial studied the safety and efficacy of post-angioplasty dissection repair using the Philips Tack endovascular system in patients with CLI and infrapopliteal disease. The Tack endovascular system is a unique specialized implantable device to optimize the treatment of dissections in patients with CLI. Endpoints included rates of major adverse events, target lesion revascularization (TLR), target limb salvage (TLS) and quality of life (QoL) metrics.

“Based on 36-month follow-up in the TOBA II BTK trial, which is following 233 patients at 41 sites internationally, the Tack endovascular system offers a new standard in repairing below-the-knee arterial dissections,” said co-principal investigator George Adams, M.D., director of cardiovascular and peripheral vascular research at UNC Rex Hospital in Raleigh, N.C., and clinical associate professor of medicine at the University of North Carolina at Chapel Hill, who presented the results to hundreds of interventional cardiologists, interventional radiologists and vascular surgeons at the New Cardiovascular Horizons (NCVH) conference in New Orleans, USA, on June 2.

Adams added: “The device stands to significantly benefit patients with CLI whose treatment with balloon angioplasty often leads to this particular complication, which typically goes untreated and unaddressed, to the detriment of long-term clinical outcomes.”

The three-year analysis of TOBA II BTK results includes the following clinical insights on the Tack endovascular system:

  • 93.9% target limb salvage in CLI patients at three years
  • 69.6% freedom from clinically-driven target lesion revascularization across all patients at three years
  • Sustained improvement in established clinical classification systems including the Rutherford clinical category and hemodynamics in ankle- and toe-brachial indices
  • Sustained improvement in patient-reported quality-of-life and mobility measures

“In treating peripheral arterial disease below the knee with balloon angioplasty, dissections of the popliteal, tibial and peroneal arteries occur with considerable frequency,” explained Chris Landon, business leader of Image Guided Therapy Devices at Philips. “With the Tack endovascular system from Philips, interventionists can reliably repair below-the-knee arterial dissections – and in doing so, improve major amputation rates and quality of life.”

Philips has previously reported data from the TOBA II and III studies, which evaluated the Tack endovascular system for superficial femoral and proximal popliteal artery dissection repair following uncoated balloon angioplasty and/or drug-coated balloon (DCB) angioplasty. These multicenter, global and European studies demonstrated that the use of the Tack endovascular system resulted in overwhelming dissection resolution following uncoated or DCB angioplasty.

  • In TOBA II, which involved uncoated and drug-coated balloons, dissection repair with the Tack System resulted in 89.6% and 86.5% 12-month primary patency (uncoated balloon group) and freedom from CD-TLR
  • In TOBA III, which involved drug-coated balloons, dissection repair with the Tack endovascular system resulted in 95.0% and 97.5% 12-month primary patency and freedom from CD-TLR

There were no major adverse events reported through 30 days in either study.

Together, the TOBA II, TOBA III and TOBA II BTK trials support the safety and efficacy of the Tack endovascular system for post-PTA dissection repair in above- and below-the-knee arterial disease. The 36-month TOBA II BTK data reported at NCVH adds to the robust body of clinical evidence supporting the safety and effectiveness of the Tack Endovascular System in both vessel beds.

Philips Tack endovascular system is currently available for sale in the USA and some EU countries. Further information, including safety information, is available here. The system is part of the company’s peripheral vascular portfolio, which includes advanced interventional imaging systems for precision guidance including Vascular Suite on its Image Guided Therapy System – Azurion; intravascular ultrasound (IVUS) catheters to assess the location of the disease and lesion morphology and guide and confirm the treatment; peripheral atherectomy devices to remove blockages; sculpting balloons to prep the vessel; and peripheral therapy devices, such as Philips’ Stellarex drug-coated balloon, to treat lesions.

[1] Hirsh AT, Jaskal ZJ, Hertzer, et al. ACC/AHA 2005 guidelines for the management of patients with peripheral arterial disease (lower extremity, renal, mesenteric, and abdominal aortic): executive summary a collaborative report from the American Association for Vascular Surgery/Society for Vascular Surgery, Society for Cardiovascular Angiography and Interventions, Society for Vascular Medicine and Biology, Society of Interventional Radiology, and the ACC/AHA Task Force on Practice Guidelines (Writing Committee to Develop Guidelines for the Management of Patients With Peripheral Arterial Disease) endorsed by the American Association of Cardiovascular and Pulmonary Rehabilitation; National Heart, Lung, and Blood Institute; Society for Vascular Nursing; TransAtlantic Inter-Society Consensus; and Vascular Disease Foundation. J Am Coll Cardiol. 2006 Mar 21;113(11):e463-654.

For further information, please contact:

Joost Maltha
Philips Global Press Office
Tel: +31 610 558 116
E-mail: joost.maltha@philips.com

Fabienne van der Feer
Philips Image Guided Therapy
Tel: + 31 622 698 001
E-mail: fabienne.van.der.feer@philips.com

About Royal Philips

Royal Philips (NYSE: PHG, AEX: PHIA) is a leading health technology company focused on improving people’s health and well-being, and enabling better outcomes across the health continuum – from healthy living and prevention, to diagnosis, treatment and home care. Philips leverages advanced technology and deep clinical and consumer insights to deliver integrated solutions. Headquartered in the Netherlands, the company is a leader in diagnostic imaging, image-guided therapy, patient monitoring and health informatics, as well as in consumer health and home care. Philips generated 2021 sales of EUR 17.2 billion and employs approximately 79,000 employees with sales and services in more than 100 countries. News about Philips can be found at www.philips.com/newscenter.

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Non-Enegry Sector I-Usahawan Programme

Darussalam Enterprise, DARe welcomes more youth participation in the Non-Energy Sector i-Usahawan Programme. It is to support the government's efforts to build a business ecosystem that will enable youths to thrive and achieve Wawasan Brunei 2035.

DARe in its Press Release has informed that youth entrepreneurs can get access to business opportunities from participating clients through DARe links Portal@darelinks.dare.gov.bn. For more information, visit www.dare.gov.bn/iusahawan or email darelinks@dare.gov.bn.

Source: Radio Television Brunei

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Musabaqah Murattal Al-Quran

10 participants took part in the Musabaqah Murattal Al-Quran and Memorisation of Al-Quran Verses for Mualaf or new converts for the Temburong District Level, yesterday morning. The competition organized by the Islamic Dakwah Centre was held at the Mukim Bokok Community Hall, Temburong District.

Emerging Champion in the Male Murratal Category was Awang Mohammad Jaya bin Mohammad Basri while Dayang Nurul 'Ain binti Mohammad Redzuan won the Female Murattal Category.

Meanwhile, for Memorisation of Al-Quran Verses, the Men's Category was won by Awang Muhammad Irfan Hamizan bin Abdul Rahim and Dayang Nurul Ayuni was champion in the Women's Category.

Source: Radio Television Brunei

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U.M.A.T Launching Ceremony and Certificate Presentation

Various skills such as basic counselling, helping, stress management and decision making are among those acquired by the participants of the Basic and Advanced Counselling Skills Course. The 8-day course ended with the closing ceremony and the establishment of 'Rakan Untuk Mu Amalan Terpuji- U.M.A.T', UNISSA.

U.M.A.T was launched by Doctor Haji Norarfan bin Haji Zainal, Rector of UNISSA. U.M.A.T is similar to peer guidance at schools in the country. The ceremony coincided with the presentation of certificates to 37 students.

Source: Radio Television Brunei

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Opportunity to Visit Nabawi Mosque

Being at the holy city of Madinah is a golden opportunity that should not be wasted. Several historical sites will become the focal point of intending pilgrims, and one of it is the Nabawi Mosque where they will have the chance to visit and perform prayers at one of largest mosques in the world.

One feels calm when stepping into the mosque. This is where Prophet Muhammad SAW and his loyal companions, Sayyidina Abu Bakar and Sayyidina Umar are buried.

Touching on the Nabawi Mosque's structure, ample space are available for congregants to pray and others. 250 giant umbrellas of over 45 metres high will open up around the mosque compound to shelter pilgrims from the sun and rain. The mosque also has 9 grand and magnificent minarets, a symbol of Islam's greatness and solidarity. Intending pilgrims will surely be captivated by the beauty of the Nabawi Mosque, especially for those who will be at the holy land for the first time.

Source: Radio Television Brunei

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Doa Selamat for Intending Pilgrims

A Doa Selamat ceremony was held for intending pilgrims from the Ministry of Culture, Youth and Sports and its departments.

In attendance was Yang Berhormat Awang Haji Nazmi bin Awang Haji Mohammad, Minister of Culture, Youth and Sports. The function that took place at the ministry coincided with a donation presentation to the intending pilgrims.

Source: Radio Television Brunei

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United States Department of States Counsellor Media Briefing

Defence, business, economic and diplomatic relations between United States and Brunei Darussalam is growing significantly. The United States Department of States counsellor stated the matter in a media briefing yesterday afternoon after concluding a two-day official visit to the country.

Source: Radio Television Brunei

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Preparation of Acute Treatment Assessment Room

Medical officers of the Brunei Darussalam Haj Management Office have prepared an acute treatment assessment room for intending pilgrims. It is located at Dallah Taibah Hotel in Madinah Al-Munawah.

Medical officers have made thorough preparations before the arrival of the intending pilgrims to the holy land. All medicines were also inspected for those in need. In an interview, Awang Haji Muhammad Shahril bin Haji Ali, head nurse of the country's haj management office delegation said they also have to ensure that medical equipment and consumable items are adequate and in good condition.

Source: Radio Television Brunei

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Media Conference on Latest COVID-19

518 new COVID-19 cases were reported yesterday, in which 513 were results from ART tests, and 5 others were from 643 RT-PCR laboratory tests. This brings the country's total cases to 153,611. This was stated by the Minister of Health at a media conference on the latest COVID-19 situation THIS afternoon at Dewan Al-Afiah, Ministry of Health. Yang Berhormat Dato Seri Setia Doctor Awang Haji Awang Mohd Isham bin Haji Jaafar stated that 71.8 percent of the total population received the third dose of the vaccine.

1 case is in Category 5, and 1 case is in Category 4. 317 cases have recovered, bringing the total recovered cases to 150,550. 2,836 cases remain active, in which 23 cases are currently treated in hospitals, whereas 2,813 others are currently undergoing home self-isolation.

Source: Radio Television Brunei

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Voluntary 2nd COVID-19 Booster Vaccination Commences On 15 June

The Minister of Health also shared that the administration of the second COVID-19 booster vaccination will be opened voluntarily starting 15th June 2022. This is taking into account the findings of scientific studies that show the elderly and those with immunocompromised conditions are at higher risk of getting severe effects from COVID-19 infection despite having received the first booster vaccination.

The second booster vaccination will be opened for adults aged 80 and above; adults aged 60 and above and with chronic diseases; those who are aged 18 above with immunocompromised conditions; and healthcare workers and frontliners who are exposed to high risk infection. The administration of the second booster dose of COVID-19 will be available at vaccination centres and will only be administered five months after the first booster dose of COVID-19. Individuals who meet the above criteria are welcome to get this extra dose.

Source: Radio Television Brunei

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