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Medical Marijuana Inc (OTCMKTS:MJNA) Finalizes Deal With Salvation Botanicals, Ltd.

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Medical Marijuana Inc (OTCMKTS:MJNA) has finalized a deal with Salvation Botanicals, Ltd. to manufacture offerings in Canada. As it is known Salvation Botanicals marks as a known extraction and formulation firm in Canada. More recently, Deloitte posted a reported stating that Canadians spend on cannabis products is expected to go up to $7 billion in 2019, as compared to expected spend of $5 billion on liquor. Overall cannabis consumption is expected to jump by up to 35%.

The highlights

Dr. Stuart Titus, the CEO of Medical Marijuana, expressed that they are finalized to sign this deal and bring their services into the Canadian market, particularly with a valued associate such as Salvation Botanicals. The cannabis market in Canada is estimated to increase over the next year and they are expecting to offer the Canadian industry with the best products available.

Kenneth Smith, the Director of Canadian Operations at Medical Marijuana, expressed that they are pleased to cherish this new global prospect and lead Canada’s new recreational industry. Salvation Botanicals comes in the list of highly reputable firms in Canada and they consider that together they can become pioneers in cannabis education during this period of historic transition.

More recently, Medical Marijuana reported that the firm and its subsidiary unit Kannaway® have recorded the best unaudited sales month in their history. This remarkable performance came this year in August. The company reported that it has established new milestones for monthly sales bookings for three successive months. Its subsidiary Kannaway® monthly sales bookings has been showing remarkable performance since last nine months.

Dr. Stuart Titus, the CEO of Medical Marijuana, expressed that they are thrilled to report August 2018 as the largest sales month in their history. There is considerable growth taking place in the market and they are delighted to be a part of that.

*Past performance is not a predictor of future results. All investing involves risk of loss and individual investments may vary. The examples provided may not be representative of typical results. Your capital is at risk when you invest – you can lose some or all of your money. Never risk more than you can afford to lose.By submitting your information you agree to the terms of our Privacy Policy • Cancel Newsletter Any Time.This is a FREE service from Finacials Trend. Signing up for our FREE daily e-letter also entitles you to receive this report. We will NOT share your email address with anyone.

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Pyxis Tankers Inc. (NASDAQ: PXS) Sells Two Small Tankers for $8.9M and Takes Delivery of Pyxis Lamda

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Pyxis Tankers Inc. (NASDAQ: PXS) has announced an agreement to sell two small tankers, Northsea Beta and Northsea Alpha. The product tanker firm will sell the two 2010 constructed 8,600 dwt product tankers for a cash consideration of around $8.6 million. Pyxis has a modern fleet of seven tankers dealing with refined petroleum products and bulk liquids transportation.

Pyxis expects net proceeds of $2.8 million. 

The sale of the vessel is expected to be completed between late January and towards the end of February 2022, pursuant to standard closing conditions. Following the discharge of the outstanding loans securing these boats and the settlement of other transaction expenses, Pyxis Tanker anticipates earning net cash proceeds of $2.8 million, which will be put into working capital. As a result, the company forecasts a $2 million non-cash loss from asset sales for the fiscal period ending December 31, 2021.

Valentines Valentis, Chairman and CEO of Pyxis Tankers, commented, “The sale of these non–core assets underscores our strategic focus on the eco–MR product tanker sector, reduces outstanding debt and improves balance sheet liquidity. Moving forward, we will have a fleet of five MRs with an average age of 8.3 years. Upon completion of the dispositions, our total debt should be approximately $77.35 million at a weighted average interest rate of less than 4% per annum with the next bank loan maturity scheduled in 3.5 years.”

Pyxis acquired Pyxis Lamda for $32 million 

Recently the company disclosed that according to a previously announced transaction, it has taken delivery of Pyxis Lamda. Pyxis Lamda is a 2017 built 50,596 dwt mid-sized product tanker that was acquired from an entity with links to the company’s CEO and Chairman for $32 million. 

Valentis commented, “We are pleased to announce the successful delivery of the Pyxis Lamda, which increases our fleet to a total of seven vessels, including five modern eco- MR2’s. The addition of this young vessel to our fleet positions the Company to take advantage of an anticipated improving chartering environment within the product tanker sector.

*Past performance is not a predictor of future results. All investing involves risk of loss and individual investments may vary. The examples provided may not be representative of typical results. Your capital is at risk when you invest – you can lose some or all of your money. Never risk more than you can afford to lose.By submitting your information you agree to the terms of our Privacy Policy • Cancel Newsletter Any Time.This is a FREE service from Finacials Trend. Signing up for our FREE daily e-letter also entitles you to receive this report. We will NOT share your email address with anyone.
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Zynerba Pharmaceuticals Inc. (NASDAQ: ZYNE) Offers Program Updates On Evaluation Of Zygel In ASD, 22q. DEE And FXS

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Zynerba Pharmaceuticals Inc. (NASDAQ: ZYNE) has given program updates for autism spectrum disorder(ASD), Fragile X syndrome (FXS), developmental and epileptic encephalopathies (DEE), and 22q11.2 deletion syndrome (22q).

Zynerba hits various milestones in Zygel development 

Armando Anido, the CEO and Chairman of Zynerba stated, “Committing to a Phase 3 development program for patients with autism spectrum disorder is a key step in the advancement of a new treatment option for patients who have high unmet medical needs and limited FDA approved treatment options. Data from our ASD clinical development program to date are compelling and, with a clear regulatory path toward potential approval, we are excited to move forward with this program.”

 “In addition, we are making good progress towards completing enrollment in the INSPIRE trial for patients with 22q11.2 deletion syndrome and expect to have topline results mid-year 2022. Putting resources behind a second indication beyond FXS and completing the INSPIRE trial is consistent with our mission of being a leader in rare and near-rare neuropsychiatric disorders,” concluded Anido

Zynerba evaluating Zygel in various indication s

Regarding the ASD program, the company plans to commence two phases three trials in 2H 2022 to evaluate Zygel in ASD. Zynerba is finalizing the third phase study protocol and will submit an IND to start the pivotal program. Also, the company is evaluating Zygel in FXS, and it expects topline RECONNECT results in 2H 2023. The EMA gave the company written scientific advice offering clarity and guidance on regulatory and clinical requirements to submit an MAA for Zygel in the treatment of behavioral symptoms related to FXS in the EU. 

Zynerba is planning to screen and enroll subjects in a 14-week open-label second phase INSPIRE study evaluating Zygel in 22q and anticipates topline results by mid this year. In addition, in Q4 2021, the company commenced more clinical sites in the US to finalize enrollment. 

Lastly, in the DEE program, the company has received FDA feedback showing that picking a specific DEE syndrome is necessary for a pediatric epilepsy indication instead of evaluating improvements in seizures in all DEEs.

*Past performance is not a predictor of future results. All investing involves risk of loss and individual investments may vary. The examples provided may not be representative of typical results. Your capital is at risk when you invest – you can lose some or all of your money. Never risk more than you can afford to lose.By submitting your information you agree to the terms of our Privacy Policy • Cancel Newsletter Any Time.This is a FREE service from Finacials Trend. Signing up for our FREE daily e-letter also entitles you to receive this report. We will NOT share your email address with anyone.
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Amyris Inc. (NASDAQ: AMRS) And ImmunityBio (NASDAQ: IBRX) Close Joint Ventures Agreement To Accelerate Next-Gen COVID-19 Vaccine Development

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Amyris Inc. (NASDAQ: AMRS) and ImmunityBio (NASDAQ: IBRX) have announced the closing of a previously announced JV agreement to expedite the commercialization of a flagship next-gen COVID-19 vaccine. 

JV combines Amyris and ImmunoBio’s vaccine capabilities 

The joint venture brings together critical vaccine technologies and production capabilities from Amyris and ImmunityBio. The goal joint venture is to commence delivery of the second-gen vaccine in 2022 as soon as practical after successful human clinical studies and regulatory authorization, with the intent of giving COVID-19 immunity and availability to underserved regions of the globe where present vaccine innovation is challenged because supply chain and cost limitations.

ImmunityBio Executive Chairman and Globa Chief Scientific and Medical Officer Patrick Soon-Shiong said, “We are pleased to combine our expertise in human trials, T-Cell technology, and our access to RNA manufacturing capacity with the Amyris and Infectious Disease Research Institute (IDRI) RNA technology platform and Amyris’ adjuvant technology. Combined, we have a real opportunity to provide true immunity against COVID-19 variants along with a platform that can quickly adapt to a future potential respiratory virus.”

Amyris to combine its RNA tech with ImmunityBio’s expertise 

Amris, the CEO and President, John Melo, said, “Combining our RNA technology with ImmunityBio’s expertise and access has the potential to significantly accelerate and de-risk our time to market for a much-needed second-generation COVID-19 vaccine. We are very pleased with the progress our teams have made in the short time we’ve been working together and remain focused on completing successful human trials as quickly as possible.”

IDRI CEO Corey Casper commented, “Two years into the COVID-19 pandemic, it has become abundantly clear that next-generation vaccines will be required to put the pandemic behind us. Vaccines that are accessible to every person across the globe, broad in their protection against current and future variants of concern, and invoke durable protective immunity are now within our reach. The ability to ‘mix and match’ vaccine platforms through this new joint venture and ImmunityBio’s multiple COVID vaccine platforms represents one of the most exciting approaches to ending COVID-19.”

*Past performance is not a predictor of future results. All investing involves risk of loss and individual investments may vary. The examples provided may not be representative of typical results. Your capital is at risk when you invest – you can lose some or all of your money. Never risk more than you can afford to lose.By submitting your information you agree to the terms of our Privacy Policy • Cancel Newsletter Any Time.This is a FREE service from Finacials Trend. Signing up for our FREE daily e-letter also entitles you to receive this report. We will NOT share your email address with anyone.
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