@rigatoni33@rigatoni33 …from iHub a dozen years ago? Good to see you. In fact, saw a post back pre-BHVN on your board about PRTG. Did some DD, liked the management. Bought in for that ride. In this one now. Eyes on SITC in November.
$PRTG @PortageBiotech some very good news coming out today at #ASCO2023. #iNkt “Several target lesions were substantially reduced in size or completely resolved, and a majority of target lesions being clinically stable after twelve weeks,” said Dr. Ian Walters.
$PRTG @PortageBiotech some very good news coming out today at #ASCO2023. #iNkt “Several target lesions were substantially reduced in size or completely resolved, and a majority of target lesions being clinically stable after twelve weeks,” said Dr. Ian Walters.
We’re pleased to share updated interim data on our lead #iNKT engager in a Phase 1/2 study for the treatment of #melanoma and #NSCLC at #ASCO23. For more details on the poster, click here: https://t.co/urrMMYy3zB
$PRTG. @PortageBiotech We’ve been waiting a very long time for good news. The abstract certainly points to that. And while there were 2 CR, 1 PR, it’s the 10 SD. Is that something we’re gonna like? A lot? Hey Ian, would you host a q and a for investors after #ASCO?
$PRTG Ian walters CEO of portage is on this panel to discuss the next innovations in medicine and primarily the future of immuno-oncology (inkt )
right after there asco poster release on the 3rd June 😉
#ASCO23
@JacobPlieth $PRTG early stage in p1/p2 ,wont necessary see the press others receive,their abstract is worth a look
Strong early efficacy results at low/mid dose in their inkt agonist treating nsclc stage 4.
Patients had not repsonded to previous therapies and PD-1.
https://t.co/evsN8KbsVA
$PRTG huge PR coming in the next week or so on early efficacy seen in their lead #inkt asset imm60.
NSCLC
100% patients prior pd-1
No grade 3-5
19 lesions (2CR /10 SD /1 MR /6 PR
All at low/ mid dose range
Results be it early are up there with KEYTRUDA! $21bn pa drug!
#ASCO23
To note stable disease(SD) in 10no lesion given this is stage 4 nsclc patients is equally as credible at their low dose (1-3mg) imm60 could be a tangible alternative to both chemo and or PEM . 12month progression free survival will be very telling $PRTG
$PRTG “well tolerated” “no MTD was determined” “2 lesions completely resolved” we can’t forget these patients have sadly been through several other treatments that failed. Well done @PortageBiotech you seem to be improving outcomes with PORT2 🙏 #ASCO23#CancerResearch
Take a listen and realise the potential of $PRTG. At this price it's the bargain of the century. ASCO is weeks away where the data will prove the investment.
$PRTG are excited to be presenting an update on our study of PORT-2 (#iNKT engager) for the treatment of #NSCLC & #melanoma at @ASCO, us investors have waited years for this data, time is now!
CA is poised to be the 4th largest economy in the world, has the highest GDP of any state, & the most small businesses in the U.S.
At the @MilkenInstitute Global Conference, Governor @GavinNewsom highlighted CA's commitment to expanding freedom & economic opportunity for all.
$PRTG This is it! I know a number of investors have been waiting to see this. Coincides with the ASCO conference poster. We get solid update on IMM60 alone and in combo with Keytruda, I’ll be a very happy investor.
$PRTG
Boom!
Global trial site updated with June 5th start.
This is running in parallel with the going p1/p2 uk arm of the trial.
Data is coming ! And quick with 12 new trial locations in the US and spain.
Merck collab is really kicking into action now $MRK
$PRTG to remind people who may not be familiar with how stacked this pipeline is with both blockbuster assets fully owned!
Inkt PORT2&3(100% owned)
adenosine PORT6&7 (100% owned)
INT230-6 PORT 1 (8% owned)
SAUG 1 -PORT 4 (70% owned)
STing VLP - 5 (44% owned)
$PRTG Investors are at the start of data rolling in. ASCO in a June we get data on Port-2 alone and in combination with Keytruda. The cohort is small, larger trial starts June, more data at SITC in Nov. And funny, the trial was designed by Merck. This year could see a breakout.
$PRTG
Unlike other biotechs portage have designed import-201 trial to meet the exact clinical requirements $BMS & $MRK require. It helps when the chairman worked at BMS / brought nivolumab to market!
https://t.co/oP7ipweTiZ