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Cannabis stocks/companies getting some major love from on Closing Bell CNBC. CEO's of Tilray and Aphria are currently being interviewed regarding New Jersey's decriminalization, as well as general growth, expansion and expansion in to new areas and markets.
Thanks for sharing Jimmy!
If only we knew where this will settle I’d say it’s a good buying opportunity.
What a bloodbath today is! I track 52 stocks every single one is in the red. Horrible day ! I’m glad I don’t hold anything on Margin.
Who are the SIX?
Do you recall if the execution indicated Form T?
Here's a bit on Form T's...I hope this helps....at least somewhat.
To avoid creating “an unbalanced market”, market makers often do not report certain trades during the day to the public and then use a T Trade not to “scare” investors into thinking a market for that stock is going in one direction or the other at the spurring of one large investor.
What is a Form T-Trade?
There is much confusion and rumor regarding “T Trades” in the penny stock market. Nasdaq Pink Sheet stocks often close at a certain price and, within 3-10 minutes after the closing bell, will show a large final trade that gets labeled as an “after hours” trade. Simply put, this is an inaccurate description of that trade.
To understand how this trade works, one must understand the role of the market maker. The most frustrating aspect of investing in the pennies, is market maker manipulation of the stock price. Anyone that claims this manipulation doesn’t happen truly does not understand the OTC Market. Market makers are in place to “control” the price of a stock and, theoretically, to ensure that the market reacts properly to supply and demand for a certain stock. Unfortunately, when large sums of money and a lack of regulation are involved, more often than not, there is manipulation that suits the needs of certain investors or the market makers themselves. After all, they are in business to make money as well. If the average investor is purchasing stocks in the OTC Market, that investor is truly at the mercy of the market makers involved in the purchase and sale of that security.
Nice post Jimmy!
Great perspective OE...thanks for bringing forth the realities of today's investment and trading mind sets.
GLTA!
3BB
Nice clip
Look forward to your return LJ. Would love to come join you!
Best idea all day long...take good care of yourself....
If I remember correctly 106/Russia and 54/US...total 160
Where have you been ogre? LOL If you get a chance catch up on all of yesterday's earlier posts. Lots of posts regarding this topic.
GLTA!
OPTEC Subsidiary Z2O Launches Vendor On-Boarding Program of Uber Type On-Demand App For Pandemic Sanitization & Cleaning In Austin Texas
CARLSBAD, CA / ACCESSWIRE / February 19, 2021 / OPTEC International, Inc. (OTC PINK:OPTI), a developer of UV and UV-C safety products using related advanced technologies specific to Personal Protection Equipment (PPE), today released the Z2O PRO App on the Apple store to begin marketing and onboarding for Z2O cleaning and sanitization professionals in the Austin, Texas area, with a particular focus on pandemic related services.
Z2O is now available for the onboarding of all cleaning and disinfecting service providers in the Austin, Texas area. This presents an opportunity for small, local cleaning companies and larger national franchise companies to enroll as a Z2O vendor in Austin, Texas. Providing a boost to cleaning businesses in the Austin area, Z2O will help assist locals in generating income during this most difficult time; not only with the pandemic, but with the current devastating weather conditions blanketing the state of Texas.
The Z2O PRO App is currently only available in the Apple Store, with availability in the Google Play Store coming in the very near future.
Z2O will be launching live in Austin, Texas on or before March 30tht 2021 for consumer services, with a target launch in Miami, Florida on or before March 22nd 2021, and several other locations shortly thereafter.
About Z2O
During these challenging times, there is a vital need to protect businesses and homes from harmful bacteria, viruses, and everything in between. Z2O is a new, on-demand app, delivering an effortless way to schedule cleaning and disinfecting services using smart devices, at the same time providing existing companies and starts ups new opportunities to create jobs and operate and expand business services. This is like the Uber of cleaning and disinfecting, offering the opportunity for the local workforce to have the ability to generate income for essential services that will help their local community as well as expand job opportunities for their employees and staff.
What the heck?
Fisker initiated with a Buy at R. F. Lafferty; tgt $23
3:29 PM ET 2/17/21 | Briefing.com
. R. F. Lafferty initiates FSR with a Buy and price target of $23. Analyst Jaime Perez commented, "Fisker Inc. (NYSE: FSR) is a California-based designer and developer of premium electric vehicles (EV). The company is developing the Fisker Ocean, an all-electric midsize luxury SUV for the consumer market with an MSRP between $37,499-$69,900. The market for EVs (electric vehicles) has increased dramatically over the past several years as customers migrate from fossil-fueled transportation to green energy transportation. The main reason for the higher demand for EVs is climate change concerns among consumers. However, consumers have been slow to adopt EVs primarily because of driving distance limitations and extended battery charging time. The goal of the company is to become a "premium automaker producing more than 100,000 units". Fisker will introduce a prototype of the Ocean all-electric SUV in mid-2021. Then, the company will launch production of the Ocean in late 2022. We are initiating coverage of Fisker Inc. (NYSE: FSR) with a Buy rating and a $23 per share price target. Our price target is based on 7.5x EV/EBITDA multiple and 2023E Sales of $310 million."
Hello AITX followers. Apologies, I am new to the company. Have spent much of the day doing DD. Looks like a worthwhile buy to the plus side, clear upward trend. Fairly certain the most recent gaps will have to be filled thought (IMHO)...I could very well be totally wrong. Doubt mm will let it run without it though....unless talks with tesla prove more substantive in the relative near term and of course any other Fortune 100 announcement. Anyhow, I'm excited to watch what happens over the next several months.
P.S. If anyone has any additional dd other than IHUB read, Reddit and of course the most recent PR's published please PM me. I look appreciate as much insight as possible.
Thank you in advance!
3BB
Love it Coop!
Fortunately I'm in at most of my holdings bottoms. Just hard to see significance of down versus up days. I feel good about the DD and buy in points. Tomorrow is a new day and hopefully the sun will be shining!
Love your posts Prov...
3BB
Mine too...not a good Thursday for my portfolio. Always springs back though. Solid DD and know what you own!
Happy Days to Come!
3BB
Any time Lily....Hope you are staying warm!
IPI-BRIc-201
Protocol name
Double-blind, placebo-controlled, randomized, multicenter Phase II study to evaluate the efficacy and safety of Brilacidin in patients hospitalized with COVID-19
Therapeutic area
Anesthesiology and resuscitation, Infectious diseases, Oncology, Therapy (general), Surgery, Cardiology, Pulmonology, Toxicology
CI start and end date
12/17/2020 - 03/31/2021
RCT number and date
No. 705 dated 12/17/2020
Organization conducting CT
Innovation Pharmaceuticals Inc. (Innovation Pharmaceuticals Inc.)
Drug name
Brilacidin
Dosage form and dosage
solution for intravenous administration, 50 mg / ml
Cities
Barnaul, Kirovsk, Moscow, Nizhny Novgorod, Ryazan, St. Petersburg, Saratov, Yaroslavl
Developer country
USA
Organization involved by the drug developer
IPharma LLC, 143026, Moscow, the territory of the Skolkovo innovation center, st. Nobel, 7, Russia
CI phase
II
KI type
IMCI
The purpose of CI
assessment of the efficacy and safety of Brilacidin in patients hospitalized with COVID-19
Number of medical institutions
20
Number of patients
106
Advantages of clinical trials in Russia
There are a multitude of factors that influence companies decisions to open clinical operations in Russia for all types of clinical trials: some of them are
Russia Clinical Trial Advantages
Data acceptance
Patient pool
Relevant investigators’ expertise, and
Cost-efficiency
Data acceptance
With adherence to global standards and regulations observed in clinical studies, The FDA and EMA accept data from such clinical trials in Russia.
Patient pool
The Russian hierarchical health care system contains a large number of health care facilities across the country which provides substantial access to various patient populations and enables rapid recruitment of study participants. Genetic diversity and high urban proportion
Investigators expertise
Access to educated, experienced, and compliant investigators who are motivated to participate in clinical trials to advance new drug development. There are GCP trained and certified Investigative Sites generating high-quality data.
Lower Costs
Russia offers lower costs for conducting clinical trials as compared to the US and Western Europe. Some of the experts have claimed that compared to the US, Russian sites offer approximately 30-60% savings to sponsors depending on the complexity of the study, study-specific procedures, patient population, and etc.
A "schedule 13G" filing is reserved for "passive investors", or those who do not intend to "exert control" in a company.
Schedule 13D filings are reserved for people or companies who may be interested in agitating for some kind of a change at the company, whereas "passive investors" are just that - passive.
What triggers a 13G filing?
Institutional investors must file a Schedule 13G within 45 days after the calendar year in which the investor holds more than 5% as of the year end or within 10 days after the end of the first month in which the person's beneficial ownership exceeds 10% of the class of equity securities computed as of the end of the....
When should we file Form 13G?
The initial Schedule 13G is due within 45 calendar days after the calendar year in which the person becomes obligated to file and amendments are due within 45 calendar days after the end of each calendar year thereafter to report any change in the information contained in the Schedule 13G.
Also read maxinvest's post 346724
IPIX
Interesting articles surfacing. Trying to piece information together. Read below...part about 10-k delay "due date relating to clinical trials in the United States and Russia"
PART III — NARRATIVE
State below in reasonable detail why Forms 10-K, 20-F, 11-K, 10-Q, 10-D, N-CEN, N-CSR, or the transition report or portion thereof, could not be filed within the prescribed time period.
Innovation Pharmaceuticals Inc. (the “Registrant”) was unable, without unreasonable effort or expense, to file its Quarterly Report on Form 10-Q (the “Quarterly Report”) for the period ended December 31, 2020 (the “Reporting Period”) by the February 16, 2021 filing due date applicable to non-accelerated filers due to a delay experienced by the Registrant in preparing disclosure relating to recent developments regarding clinical trials for the Registrant’s lead drug compound, and in particular, developments on or around the filing due date relating to clinical trials in the United States and Russia. The Registrant anticipates that it will file the Quarterly Report no later than the fifth calendar day following the prescribed filing due date.
Russia is planning to present an "antidote" to Covid-19. It is expected to be more than 99% effective. This was stated by the head of the Federal Medical and Biological Agency Veronika Skvortsova, according to the website of the Russian government.
It is also planned to release one more unique medicine.
Related: UK approves AstraZeneca vaccine against Covid-19
"Both are unique and have no analogues in the world. The drug that I would like to talk about is the first etiotropic drug that directly affects the virus. In fact, it is an antidote to coronavirus infection," Veronika Skvortsova said.
Related: Ukraine needs to develop rules for coexistence with Russia as neighbor, - Foreign Minister
The effectiveness of this "antidote" in preclinical trials was up to 99%. If clinical trials are successful, it will be the world's first direct-acting antiviral drug.
The second drug is being developed to treat severe complications of coronavirus infection - a cytokine storm or an abnormal response of the immune system. This drug has already passed clinical trials and is at the last stage of registration.
PART III — NARRATIVE
State below in reasonable detail why Forms 10-K, 20-F, 11-K, 10-Q, 10-D, N-CEN, N-CSR, or the transition report or portion thereof, could not be filed within the prescribed time period.
Innovation Pharmaceuticals Inc. (the “Registrant”) was unable, without unreasonable effort or expense, to file its Quarterly Report on Form 10-Q (the “Quarterly Report”) for the period ended December 31, 2020 (the “Reporting Period”) by the February 16, 2021 filing due date applicable to non-accelerated filers due to a delay experienced by the Registrant in preparing disclosure relating to recent developments regarding clinical trials for the Registrant’s lead drug compound, and in particular, developments on or around the filing due date relating to clinical trials in the United States and Russia. The Registrant anticipates that it will file the Quarterly Report no later than the fifth calendar day following the prescribed filing due date.
Daily volume has significantly increase since JAN 15 to present.
Competition
The Global Supply Chain management area has many different entities, all competing. Some are very large. However, our model is significantly different from most of the providers already operating.
To be successful in the global supply chain management area, a company must be involved in planning the function of the entire process, from start to finish, or end to end. We intend to concentrate our model on the cannabis, nutraceutical, pharmaceutical and cosmetic areas. We believe this makes our approach unique and distinguishable at this time.
There is no guarantee that a larger, more fully funded, company will determine to seek to gain access to the same business.
Intellectual Property
Our Global3pl SAAS Platform is a proprietary software developed by the Company. The SaaS-based platform ecosystem will fully integrate all aspects of the Cannagistics operations, from receiving raw materials for clients, through product manufacturing, document compliance, distribution, and shelf-life batch tracking.
We have plans to develop a GMP certified biotech lab in Malta with a fundamental skill in initially the cosmetic and then potentially the medicinal, nutraceutical and cannabis/hemp/CBD industries. Our plan is to have this Malta lab cater to customers in the EU. We also plan to potentially have other facilities that will cover our target customers in the US, Canada and Columbia, potentially located in Baton Rouge, Toronto and Bogotá, respectively.
If we are successful in fully developing such capabilities we intend to seek out and employ a team of a multidisciplinary professionals in the pharmaceutical, nutraceutical and over the counter industries, and utilize complex supply chain and logistics management, unique technology and intellectual property. Cannagistics’ Lab’s purpose is to add value and offer a progress proposal to the Malta medicinal cannabis industry, based on its interest to support, educate, take advantage of and focus on the development of potentially breakthrough medicinal cannabis products with different therapeutic uses in patients around the world to whom science and traditional medicine simply could not reach. Such products will be subject to testing and certification from various governmental agencies, which may be a difficult expensive and time-consuming process. Our vision and knowledge will potentially focus on GMP biopharmaceutical cannabis-based medicines, - with the highest standards starting from the raw material - for multiple applications in patients, using latest technology, ancestral knowledge, scientific studies, with an exceptional team of research and development following the strictest standards and good distribution practices for export and national use.
This post should be pinned. Best advice for all to follow and not forget.
ETRADE looking to dump 1mm shares at .01437
I'm sure this question has already been asked and answered so apologies in advance for asking again....
....any idea when we might find out about EUA approval status?
TIA
3BB
Is there a link between Carnegie and Renewal Fuels, Inc...RNWF? Somebody on Twitter posted to his twitter feed....JC
TIA,
3Bb