Register for free to join our community of investors and share your ideas. You will also get access to streaming quotes, interactive charts, trades, portfolio, live options flow and more tools.
Insiders own a fair share of this little beauty, might add more to the stash as these prices are cheap $$$$$$
Time to load, directors have been purchasing shares, 4x upside here, their science could be a huge success $$$$$$
Its been under 3$ lol
IMMX showed some spark this morning. I was kind of surprised.
Stock had some nice volume Friday.
Curious what’s going on behind the scenes.
Watch out when the insiders buy more, it’l pop to 5/6 again, these 2’s are a easy double
These are cheap now, buy em up folks $$$$$$$
Been adding this, updates should commence soon $$$$$$
Interesting dip this had, loaded more
Dropping like a rock, 2$ is a buy barring any bad news that leaked out
Stock has been crushed waiting to see if 2.50 holds watching
Insiders did not flip any shares! Very good hold here
Back to $5- highest mark in 2 years.. IPO price..
$IMMX current valuation with everything the way it is. should be 300-500 m ..
as far as technicals.. great current chart..
an increase of volume should propel this to 5 (which was the IPO price) and an test of the 7.5-9 area before end of year..
good luck to all.
Careful,dilution could happen anytime here. We sold out completely. Will watch this for awhile
Under 3 again it seems, insiders selling off?? Again! Probably in kahoots with hedge fund managers. This should be well over 4$ an it cannot hold, red flag again, we’l see
Next big bio here, huge upside possible. Adding here again to the stash
NEWS Immix Biopharma Announces Complete Response in 9th Relapsed/Refractory AL Amyloidosis Patient in NXC-201 Clinical Trial at IMS 20th Annual Meeting
100% (9/9) overall response rate and 67% (6/9) complete response rate (MRD 10-5) observed in heavily pre-treated patients with daratumumab relapsed/refractory AL Amyloidosis as of the September 20, 2023 data cutoff
100% (4/4) overall response rate and 75% (3/4) complete response rate observed in t(11;14) relapsed/refractory AL Amyloidosis
Best responder duration of response was 19.2 months with response ongoing; median follow-up of 7.3 months (range: 2.5 – 16.5 months) as of the data cutoff date of September 20, 2023
ImmixBio plans to submit a BLA for FDA approval in AL Amyloidosis once 40 patients are treated with NXC-201
The expected primary endpoint for NXC-201 in relapsed/refractory AL Amyloidosis is overall response rate
LOS ANGELES, Oct. 03, 2023 (GLOBE NEWSWIRE) -- Immix Biopharma, Inc. (“ImmixBio”, “Company”, “We” or “Us”), today announced presentation of additional AL Amyloidosis clinical data from its Phase 1b/2a NEXICART-1 (NCT04720313) study of novel, autologous, BCMA-targeted chimeric antigen receptor T (CAR-T) cell therapy, NXC-201, at an oral presentation at the 20th International Myeloma Society Annual (IMS) Meeting being held in Athens, Greece on September 27-30 2023. One new patient and additional follow-up data from an additional 8 patients (9 total) are included in this update. All patients were DARZALEX ® (daratumumab) combination therapy relapsed/refractory and experienced a median of 6 earlier treatments that failed to stop worsening of disease (lines of therapy) prior to receiving NXC-201.
“There are no approved drugs for relapsed/refractory AL Amyloidosis,” said Polina Stepensky, M.D., Director of the Hadassah Medical Organization’s Department of Bone Marrow Transplantation and Immunotherapy for Adults and Children, and principal study investigator. “NXC-201’s 100% response rate in relapsed/refractory AL amyloidosis patients, including t(11;14) and cardiac involved, indicates a potential broad mechanism of action. Additionally, as a one-time treatment, NXC-201 would present an attractive alternative to multi-drug combination, long-term daily or weekly regimens for relapsed/refractory AL amyloidosis patients.”
“Currently, AL Amyloidosis treatment involves repeat dosing and weekly distant travel to academic medical centers,” said Ilya Rachman, M.D., Ph.D., Chief Executive Officer of Immix Biopharma. “One-time treatment with NXC-201 could fill the void for relapsed/refractory AL Amyloidosis, where there are no therapies approved today, while restoring quality of life.”
Gabriel Morris, Chief Financial Officer of Immix Biopharma, added, “NXC-201’s uniquely favorable CAR-T tolerability profile and an apparent ability to clear disease-causing amyloid chains from the body within ~30 days could make it particularly suitable for treatment in a potential outpatient setting.”
kind of a Perfect Storm..
-great chart- 52 week high, with B/O on daily and weekly
-increased volume
-strong insider buying
-very low float and market cap..
-very strong trials on FDA Orphan drug designated products. .
Immix Biopharma Announces 72-Patient NXC-201 Clinical Data at the IMS 20th Annual Meeting, 95% Overall Response Rate in Multiple Myeloma
Yahoo Finance
Yahoo Finance
Sign in
?
Immix Biopharma Announces 72-Patient NXC-201 Clinical Data at the IMS 20th Annual Meeting, 95% Overall Response Rate in Multiple Myeloma
Immix Biopharma, Inc.
Mon, Oct 2, 2023, 5:06 AM PDT11 min read
IMMX+20.91%
Immix Biopharma Announces 72-Patient NXC-201 Clinical Data at the IMS 20th Annual Meeting, 95% Overall Response Rate in Multiple Myeloma
Immix Biopharma Announces 72-Patient NXC-201 Clinical Data at the IMS 20th Annual Meeting, 95% Overall Response Rate in Multiple Myeloma
95% overall response rate observed in relapsed/refractory multiple myeloma patients not previously treated with BCMA-targeted therapy. Median progression free survival (mPFS) was 12.9 months as of the July 17, 2023 data cut-off
90% overall response rate observed in relapsed/refractory multiple myeloma at the therapeutic dose including patients with, and without prior BCMA-targeted therapy
Class-Leading Response Rate in BCMA-exposed patients (frequently excluded from BCMA CAR-T clinical trials) has the potential to meet an important market need
ImmixBio plans to submit a BLA for FDA approval in multiple myeloma once 100 patients are treated with NXC-201
The expected primary endpoints for NXC-201 in relapsed/refractory multiple myeloma are overall response rate and duration of response
great Nexcella results.
breakout on daily and weekly chart.
low float and increased volume..
making a beeline back to ipo price of 5 and then ath 8.5
.20 from highs
Will it go to 2$ area again, triple down here
Adding to the stash, buyout candidate here, looming for 15! $$$$$$
low volume Friday..
Still near zero out side buyers and retail..
all the volume has been from within..
once the volume comes..
Followers
|
9
|
Posters
|
|
Posts (Today)
|
0
|
Posts (Total)
|
236
|
Created
|
12/17/21
|
Type
|
Free
|
Moderators |
Volume | |
Day Range: | |
Bid Price | |
Ask Price | |
Last Trade Time: |