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Why am I the only one posting here? This thing has been steady up over100% since I started posting here. Even on a day like today when most others are red. Another green day here!! $RYTM
When $20 breaks and holds this will fly! IMO
Looking like it’s ready to move up again here. Possible bounce off of support.
Some you win some you lose - I had a lot of conviction but later lost faith after that time and sold completely.
Thanks for posting. Breakout mode! GL
I lost money on RYTM and booked losses already.
In my view ORMP is better than RYTM from investment perspective.
The current market capon $255 million allows it to be a 10 bagger ($2.55 B) - speciall that it has first in class product and huge unmet market.
RTYM also has first in class product with unmet needs but it is rare disease and not many outside US can afford
Agree - it is good company
Will take time to make money but proof of product is there.
The valuation is fair at this point - upside maybe 50-70% by end of the year based on how they price and are able show sale.
The payment cycle with insurance will be key as the product is very high priced -
I started building a major position. And already a little green!
Quite the biotech soon last couple weeks= opportunity!
For some reason it is tanking now -sale the news
You can actually wait for some time and buy - this is a long term play
I missed out this one!
Just amazing results - they are starting new basket trials.
The product is approved for one indication so it is now label expansion - the pricing power is amazing. This should really take off. Is it next Alexion in terms of rare disease treatment and pricing power?
Head the conf call - It was good call.
The results are much better that what PR said. Slide 14-15 shows correct numbers which were clarified by them.
Real numbers
Total patients - 31
Total BBS patients - 28
No of patients dropped - 4
Total no of patients relevant - 24
No of patients with 5%+ weight reduction - 16 = 67% that is double the number compared to combined number of 34.5%
No of patients who lost more than 10% weight - 11 out of 24 (45.8%)
Mean reduction - 14.5%
Compared to 1st approval which had few hundred population, BBS has 1000-1500 target population in US alone
This is large population for rare disease - @ $200k per year - this is a big market.
Also this is not a gene therapy - so drug is needed forever and it keeps the weight down.
Last point - All genes targeted in basket trial are in BBS category (strong or very strong relationship) so they think the basket trial results may be positive.
Cash enough till 2022. I think if stock goes down further, it will be good opportunity to buy - stock could give 50% returns from here in 6 months based on basket trial results.
Phase 3 results - BBS stat significant -AL not
Market reaction is not good. Conf call will give more info
https://finance.yahoo.com/news/rhythm-pharmaceuticals-announces-positive-topline-120000038.html
Finally - Approval
“Rhythm Pharmaceuticals Announces FDA Approval of IMCIVREE™(setmelanotide) as First-ever Therapy for Chronic Weight Management in Patients with Obesity Due to POMC, PCSK1 or LEPR Deficiency”
Another good news - voucher that they can sell or use for next approval
“With this approval, the FDA issued a Rare Pediatric Disease Priority Review Voucher (PRV) to Rhythm. The PRV can be redeemed to receive priority review for any subsequent marketing application or sold or transferred to other companies for their programs.”
https://finance.yahoo.com/news/rhythm-pharmaceuticals-announces-fda-approval-123000486.html
That’s a big run with PDUFA being in November. I took some profit but still in the game and will buy 100% back if reversal. Outstanding shares only @ 44M and float 30M. PT @ $33.
RYTM is not cheap as it has market cap of $832 million for pre-revenue biotech - so it is richly valued.
It has 70 employees - more than many biotech at this stage but not sufficient for marketing the drug. So they have to find a partner or go with buyout.
The good news is - the co has $228 milllion plus cash and it will allow them to run till end of 2021.
They are in niche area and there is no other competition nearby. If the drug can address genetic obesity - they have 80,000 target audience in US alone.
If the drug can be tested on genetic obesity/weight loss, it will be gold mine.
Not so sure the last few years. But what the heck.
I’m new on RYTM. I’ve done enough DD on PSTI and RDHL to hold a small 500 share stake in both. I’ll do some extra digging here because the stakes are much higher. The last 3 months haven’t been bad on the other two.
GLTUA
Pr
Sure. A free country, isn't it?
Can anyone play???
Thanks for the heads up Amatuer17,
i'll dig into it over the weekend.
Welcome to the board. Hope we all make money
This is a PDUFA based play
PDUFA date - 27th Nov
Disease - rare disease - obesity based on genetics
MOA - impacts the MC4PA gene that controls obesity and hunger. They have 4 more trials for other sub areas also in advance stage.
As per conf call - they are looking at pricing from $200k to $400k per year Patient population for this approval - around 1000
https://ir.rhythmtx.com/static-files/fd4e0919-4d82-47e0-afe3-8cd9b5151490
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