Intra Cellular Therapies Inc (ITCI) オプション

ITCI rangenbound

Positive topline (pump) ... immediately followed by dilution (dump).

Geez..... No posting on this stock for over 1 year...... When are people going to discover this Gem?

ITCI > diluting > shelf placement last Friday!

ITCI respecting the ma20 on the 240min chart ~

* * $ITCI Video Chart 09-09-2020 * *

Link to Video - click here to watch the technical chart video

Stock Analyzer

Gravity Analytica

Wow, $38 in December 2019 and now after FDA approval, $15 per share.

How is the underwriting going?

maybe your right

If that's the case, then maybe you should change your screen name :)

lol.

thats because I am not in, let me load the boat first then watch it drop like a rock

lol

I found that interesting as well. PPS has fallen from .45 high after FDA approval, but I thought it may drop significantly more with the offering, but...

huh? and no significant price movement


all the stocks I buy with offerings collapse

ITCI 10M share offering.

It's interesting to note that ticker ACAD, Acadia pharmaceuticals has a very similar portfolio as ITCI, Intra-Cellular Therapies Inc., it's almost as if they are two sides of the same coin.

so immature, and misleading, this is not elementary school, this is peoples lives and money

go find some internet playground other than this to play your silly games

I hear there is alot of controversy on the Rainbow Unicorns stock site, have fun over there




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* * $ITCI Video Chart 12-24-2019 * *

Link to Video - click here to watch the technical chart video

Carl Icahn took stake today

Christmas Eve run!

ITCI

50+ today

* * $ITCI Video Chart 12-23-2019 * *

Link to Video - click here to watch the technical chart video

ALL IN=$$$$

I was in and out here for a quick %25. Huge move today...

$ITCI Banked here

Analyzer suggested a buy when this was $8 with super high volatility. It was spot on.

This is precisely why my trading days begin early. Take a hint, traders.....

$40


ITCI

This will run hard

ITCI is a great $$$$$ opportunity.

“We believe CAPLYTA provides healthcare providers a new, safe and effective treatment option to help the millions of adult patients with schizophrenia,” said Dr. Sharon Mates, Chairman and CEO of Intra-Cellular Therapies. “This approval represents the culmination of years of scientific research. We are especially grateful to the patients, their caregivers, and the healthcare professionals who have contributed to the development of CAPLYTA.”

Schizophrenia is a serious mental illness impacting approximately 2.4 million adults in the United States. The clinical presentation of schizophrenia is diverse. Acute episodes are characterized by psychotic symptoms, including hallucinations and delusions, often requiring hospitalization. The disease is chronic and lifelong, often accompanied by depression and gradual deterioration of social functioning and cognitive ability. Patients with schizophrenia often discontinue treatment as a result of side effects such as weight gain and movement disorders.

“Schizophrenia is a complex disease that severely impacts patients and their families,” said Jeffrey A. Lieberman, M.D., Lawrence C. Kolb Professor and Chairman of Psychiatry, Columbia University, College of Physicians and Surgeons and Director, New York State Psychiatric Institute. “Effective treatment provided in a timely fashion can be game-changing for people living with schizophrenia. The efficacy and safety profile of CAPLYTA approved by the FDA, offers healthcare providers an important new option for treating people living with schizophrenia.”

Please also see full Prescribing Information including Boxed Warning.

Important Safety Information

Boxed Warning: Elderly patients with dementia-related psychosis treated with antipsychotic drugs are at an increased risk of death. CAPLYTA is not approved for the treatment of patients with dementia-related psychosis.

Contraindications: CAPLYTA is contraindicated in patients with known hypersensitivity to lumateperone or any components of CAPLYTA.

Warnings & Precautions: Antipsychotic drugs have been reported to cause:

Cerebrovascular Adverse Reactions in Elderly Patients with Dementia-Related Psychosis, including stroke and transient ischemic attack. See BOXED WARNING above.
Neuroleptic Malignant Syndrome, which is a potentially fatal reaction. Signs and symptoms include: hyperpyrexia, muscle rigidity, delirium, autonomic instability, elevated creatinine phosphokinase, myoglobinuria (and/or rhabdomyolysis), and acute renal failure. Manage with immediate discontinuation of CAPLYTA and close monitoring.
Tardive Dyskinesia, a syndrome of potentially irreversible, dyskinetic, and involuntary movements which may increase as the duration of treatment and total cumulative dose increases. Discontinue CAPLYTA if clinically appropriate.
Metabolic Changes, including hyperglycemia, diabetes mellitus, dyslipidemia, and weight gain. Measure weight and assess fasting plasma glucose and lipids when initiating CAPLYTA and monitor periodically during long-term treatment.
Leukopenia, Neutropenia, and Agranulocytosis (including fatal cases). Perform complete blood counts in patients with pre-existing low white blood cell count (WBC) or history of leukopenia or neutropenia. Discontinue CAPLYTA if clinically significant decline in WBC occurs in absence of other causative factors.
Orthostatic Hypotension and Syncope. Monitor heart rate and blood pressure and warn patients with known cardiovascular or cerebrovascular disease.
Falls. CAPLYTA may cause somnolence, postural hypotension, and motor and/or sensory instability, which may lead to falls and, consequently, fractures and other injuries. Assess patients for risk when using CAPLYTA.
Seizures. Use CAPLYTA cautiously in patients with a history of seizures or with conditions that lower seizure threshold.
Potential for Cognitive and Motor Impairment. Advise patients to use caution when operating machinery or motor vehicles until they are reasonably certain CAPLYTA therapy does not affect them adversely.
Body Temperature Dysregulation. Use CAPLYTA with caution in patients who may experience conditions that may increase core body temperature such as strenuous exercise, extreme heat, dehydration, or concomitant anticholinergics.
Dysphagia. Use CAPLYTA with caution in patients at risk for aspiration.
Drug Interactions: Avoid concomitant use with CYP3A4 inducers and moderate or strong CYP3A4 inhibitors.

Special Populations: Neonates exposed to antipsychotic drugs during the third trimester of pregnancy are at risk for extrapyramidal and/or withdrawal symptoms following delivery. Breastfeeding is not recommended. Avoid use in patients with moderate or severe hepatic impairment.

Adverse Reactions: The most common adverse reactions in clinical trials with CAPLYTA vs. placebo were somnolence/sedation (24% vs. 10%) and dry mouth (6% vs. 2%).

About CAPLYTA (lumateperone)

CAPLYTA is an oral, once daily medicine approved for the treatment of schizophrenia of adults (42mg/day).

The mechanism of action of CAPLYTA in the treatment of schizophrenia is unknown. However, the efficacy of CAPLYTA could be mediated through a combination of antagonist activity at central serotonin 5-HT2A receptors and postsynaptic antagonist activity at central dopamine D2 receptors.

CAPLYTA is being developed for the treatment of bipolar depression, behavioral disturbances in patients with dementia, including Alzheimer's disease, depression and other neuropsychiatric and neurological disorders. CAPLYTA has not been demonstrated to be safe and effective in these other areas. CAPLYTA was approved for the treatment of schizophrenia in adults by the U.S. Food and Drug Administration in December 2019.

About Intra-Cellular Therapies

Intra-Cellular Therapies is developing novel drugs for the treatment of neuropsychiatric and neurodegenerative diseases and diseases of the elderly, including Parkinson's and Alzheimer's disease. The Company’s first product, CAPLYTA, has received FDA approval for the treatment of schizophrenia in adults and is in development for the treatment of bipolar depression, behavioral disturbances in patients with dementia, including Alzheimer's disease, depression and other neuropsychiatric and neurological disorders. Intra-Cellular Therapies is also utilizing its phosphodiesterase (PDE) platform and other proprietary chemistry platforms to develop drugs for the treatment of CNS and other disorders. The lead molecule in the Company's PDE1 portfolio, ITI-214, is in development for the treatment of symptoms associated with Parkinson's disease and for the treatment of heart failure.

Forward-Looking Statements

This news release contains "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995 that involve risks and uncertainties that could cause actual results to be materially different from historical results or from any future results expressed or implied by such forward-looking statements. Such forward-looking statements include statements regarding, among other things, the initiation of the commercial launch of CAPLYTA, including the timing thereof, our belief that CAPLYTA provides healthcare providers a new, safe and effective treatment option to help the millions of adult patients with schizophrenia, our estimates of the number of adults in the United States impacted by schizophrenia, the safety and efficacy of CAPLYTA and our other product candidates; the potential for CAPLYTA to benefit patients suffering from a range of neuropsychiatric and neurodegenerative diseases and development efforts and plans under the caption “About Intra-Cellular Therapies.” All such forward-looking statements are based on management's present expectations and are subject to certain factors, risks and uncertainties that may cause actual results, outcome of events, timing and performance to differ materially from those expressed or implied by such statements. These risks and uncertainties include but are not limited to the following: there are no guarantees that CAPLYTA will be commercially successful; we may encounter issues, delays or other challenges in launching or commercializing CAPLYTA; whether CAPLYTA receives adequate reimbursement from third-party payors; the degree to which CAPLYTA receives acceptance from patients and physicians for its approved indication; challenges associated with execution of our sales activities, which in each case could limit the potential of our product; results achieved in CAPLYTA in the treatment of schizophrenia once we have launched the product may be different than observed in clinical trials, and may vary among patients; risks associated with our current and planned clinical trials; we may encounter unexpected safety or tolerability issues with CAPLYTA following commercial launch for the treatment of schizophrenia or in ongoing or future trials and other development activities; our other product candidates may not be successful or may take longer and be more costly than anticipated; product candidates that appeared promising in earlier research and clinical trials may not demonstrate safety and/or efficacy in larger-scale or later clinical trials; our proposals with respect to the regulatory path for our product candidates may not be acceptable to the FDA; our reliance on collaborative partners and other third parties for development of our product candidates; and the other risk factors detailed in our public filings with the Securities and Exchange Commission. All statements contained in this press release are made only as of the date of this press release, and we do not intend to update this information unless required by law.

Contacts:

Intra-Cellular Therapies, Inc.
Juan Sanchez, M.D.
Vice President, Corporate Communications and Investor Relations
646-440-9333

Burns McClellan, Inc.
Lisa Burns
jgrimaldi@burnsmc.com
212-213-0006

MEDIA INQUIRIES:

Ana Fullmer
Corporate Media Relations W2Owcg
afullmer@wcgworld.com
202-507-0130

Source: Intra-Cellular Therapies, Inc.




Primary Logo

May have some noise now

Quiet**

Pretty quit here for a spec play...

* * $ITCI Video Chart 07-23-2019 * *

Link to Video - click here to watch the technical chart video

* * $ITCI Video Chart 07-08-2019 * *

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Nice Call No Revenues Losing 141 Million Dollars a year burning cash faster then a oven VERY BLOATED Market cap here there drug just failed and there other drugs are YEARS still to be development and will cost 100s of millions dollars more and there potential sales are min at best current market cap makes zero since should trade below book value given the massive cash burn

https://seekingalpha.com/news/3291224-intra-cellular-gets-good-news-fda-related-toxicity-lumateperone-shares-ahead-33-percent

* * $ITCI Video Chart 05-01-17 * *

Link to Video - click here to watch the technical chart video

Having trouble understanding why this is trading above 10.

Nice close let's see what happens Tuesdsy

I guess if you exit at 18.1818 cents, your 1100 shares will be worth $20

13's the new 15. Soon 11 will be the new 13. And then it will fade to zero along with their cash. Drug failed. It's all over for this one trick pony

It's about to pop!

I'm in on this. I think any price at this level is a good entry.

I'm in here with 1100 starter position at $15. 23. Looking at $20 exit

Seems like this one is about to head up. Watching it for an entry point. I was busy with my other trades and missed the low. Hopefully... hopefully

Gotta WHOLE LOTTA GROUND to go to recover here. Thank you shorties!! $450+mil is nice to have in the bank here, huh? I'm thinking that's prime 'takeover territory' at current pps!!

$ITCI

There's my move!! Nice bounce off the day's low. Volume emerging too.

$ITCI