$AFMD CRR now at 77% (31 HL patients at RP2D), & it was at 70.8% (24 HL patients at RP2D). This is very good data for this population! This data would cause $BMY MCAP to increase by billions, (same for recent $ONCS data). The big pharma players are failing patients & shareholders
$AFMD/@affimed proved me right (and would do even better with more cycles, higher dose, and/or earlier line treatment) because using the new CRR, 50% of previous PR did or would (on average) turn CR.
CRR after 1 cycle (5/12)=41.66%
CRR “up to 4 cycles” (17/24)=70.83%
New data from $ONCS #Melanoma trial:
At time of surgery:
—66.7% (6/9) pathological CR (pCR)
—88.9% (8/9) evaluated patients had a major pathologic response (pMR; ≤10% viable tumor cells in the analyzed surgical specimen)
Preoperative:
—70% ORR (7/10) w/4CR+3PR+2SD, so 90%DCR!
New data from $ONCS #Melanoma trial:
At time of surgery:
—66.7% (6/9) pathological CR (pCR)
—88.9% (8/9) evaluated patients had a major pathologic response (pMR; ≤10% viable tumor cells in the analyzed surgical specimen)
Preoperative:
—70% ORR (7/10) w/4CR+3PR+2SD, so 90%DCR!
Today’s $ONCS press release also stated:
“expected pathological CR rate w/single agent nivolumab in this setting is around 30%. The pCR of 66.7% observed w/the addition of TAVO™-EP to nivolumab suggests that intratumoral expression of IL-12 is adding to nivolumab efficacy”
Today’s $ONCS press release also stated:
“expected pathological CR rate w/single agent nivolumab in this setting is around 30%. The pCR of 66.7% observed w/the addition of TAVO™-EP to nivolumab suggests that intratumoral expression of IL-12 is adding to nivolumab efficacy”
New data from $ONCS #Melanoma trial:
At time of surgery:
—66.7% (6/9) pathological CR (pCR)
—88.9% (8/9) evaluated patients had a major pathologic response (pMR; ≤10% viable tumor cells in the analyzed surgical specimen)
Preoperative:
—70% ORR (7/10) w/4CR+3PR+2SD, so 90%DCR!
Today’s $ONCS press release also stated:
-No disease recurrence has been observed at a median follow up of 7 months from the date of surgery
-One patient with a RECIST v1.1 PR
declined surgery due to significant response after neoadjuvant treatment
-No grade 4/5 adverse event
Today’s $ONCS press release also stated:
-No disease recurrence has been observed at a median follow up of 7 months from the date of surgery
-One patient with a RECIST v1.1 PR
declined surgery due to significant response after neoadjuvant treatment
-No grade 4/5 adverse event
Today’s $ONCS/@OncoSec press release also stated:
“particularly exciting that ALL patients that were predicted to be non-responders to immune checkpoint blockade by biomarker analysis prior to treatment appear to respond to TAVO™+nivolumab, supporting further the MOA of IL-12”
Today’s $ONCS/@OncoSec press release also stated:
“analysis identified four patients with low CD8+ TIL, low PD-L1 and low TIS; a biomarker signature that is negative predictive for response to immunotherapy. Of note, ALL FOUR of these patients achieved pathological CR (pCR)”
New data from $ONCS #Melanoma trial:
At time of surgery:
—66.7% (6/9) pathological CR (pCR)
—88.9% (8/9) evaluated patients had a major pathologic response (pMR; ≤10% viable tumor cells in the analyzed surgical specimen)
Preoperative:
—70% ORR (7/10) w/4CR+3PR+2SD, so 90%DCR!
$ONCS:105 patient #AdvancedMelanoma trial showed a 40.6% disease control rate (CR+PR+stable disease) in “highly refractory patient pop with no standard-of-care treatment options,” & durable responses/12+ month OS improvement/etc in patients that HAVE/WERE PROGRESSING AFTER CPI(s)
$ONCS just MET THEIR ENDPOINT & released GREAT DATA! IMO, #TAVO+#Keytruda will be authorized/approved by the @US_FDA (see DCR(40.6%)/(OS 23vs10!)/ORR/DoR/etc) for these R/R #AdvancedMelanoma patients with basically NO OTHER OPTIONS, & were truly R/R to anti-PD-1 & progressing b4!
$ONCS just MET THEIR ENDPOINT & released GREAT DATA! IMO, #TAVO+#Keytruda will be authorized/approved by the @US_FDA (see DCR(40.6%)/(OS 23vs10!)/ORR/DoR/etc) for these R/R #AdvancedMelanoma patients with basically NO OTHER OPTIONS, & were truly R/R to anti-PD-1 & progressing b4!
$ONCS just MET THEIR ENDPOINT & released GREAT DATA! IMO, #TAVO+#Keytruda will be authorized/approved by the @US_FDA (see DCR(40.6%)/(OS 23vs10!)/ORR/DoR/etc) for these R/R #AdvancedMelanoma patients with basically NO OTHER OPTIONS, & were truly R/R to anti-PD-1 & progressing b4!
$AFMD/@affimed proved me right (and would do even better with more cycles, higher dose, and/or earlier line treatment) because using the new CRR, 50% of previous PR did or would (on average) turn CR.
CRR after 1 cycle (5/12)=41.66%
CRR “up to 4 cycles” (17/24)=70.83%
@jfais20 I bet at least 50% of the PRs turn into CRs, as $AFMD/@affimed interventions have always shown deepening of responses over time, and there is no reason to believe that won’t be the case here. $AFMD should be up at least 100% right now!📈🚀
Déjà vu at $2, but this time the $2 🧲 is even more ridiculous, especially in light of the recent data and Artiva partnership🎰
P.S. IMO, $AFMD/@affimed is worth about $60 per share rn
@technology@emilychangtv gig CEOs saying make X per hour bc r only talking about when on delivery/ride, not the time spent waiting in car for offer. E.g., work 1 hour make $10,but bc did $10 order or ride in 20min, they deceive&say made $30 per hour,& say part time when working 60hrs a week
$ONCS/@OncoSec just said it will release data for two different #Melanoma trials before the end of 2022, & their previously released #Melanoma data was, IMO, definitely good enough for @US_FDA approval, especially (but not limited to) for the anti-PD-1 non responders population⏳
$ONCS/@OncoSec’s #TAVO+#Keytruda > #Keytruda, as #TAVO DEFINITELY increases ORR/OS/etc for anti-PD-1 non responders! This means $ONCS is EXTREMELY valuable, & can do 1st line!
$MRK (or $BMY, $RHHBY/@genentech, $PFE, $AZN, $REGN, $GSK, $GILD, etc) should definitely acquire $ONCS!