BREAKING NEWS: $AGEN today has been granted Patent The present disclosure provides #multispecific (e.g., bispecific) #antibodies that specifically bind to human GITR and/or human #OX40 $INCY partnered
BLAIR: #AACR21 $INCY $AGEN $MRTX $ITOS Abstract Highlights and Meeting Itinerary On Saturday, April 10, through Thursday, April 15, the American Association of Cancer Research (AACR) will host the first of two week-long virtual conferences, with the second to be hosted on Monday, May 17, through Friday, May 21. Full regular abstracts were posted to the AACR meeting website on March 10 with clinical trial and late-breaking abstracts to be released at the start of the conference, and in this note we highlight several important data presentations for our coverage list and other data of interest. In addition, an itinerary of all relevant presentations to our coverage list and the wider oncology landscape is appended at the end of this note. In particular, we highlight: • Incyte (INCY $83.18; Outperform) will be providing the first clinical update with the company’s A2A/A2B receptor inhibitor and hosting a conference call with investors (on Monday, April 12) to discuss the company’s broader adenosine targeting strategy, including a CD73 antibody. The adenosine pathway has garnered significant industry interest, and therapies targeting this pathway have led to monotherapy responses, although clear clinical development paths have yet to be established, in our opinion. • The next data point for TIGIT antibodies will come from iTeos (ITOS $34.54), which will present preliminary Phase I data with EOS884448 as a monotherapy. Recent management commentary suggests pharmacodynamic effects of EOS884448 will be focused on the periphery for the AACR presentation, with biopsy analysis coming later in the year. Recall other TIGIT antibodies have shown minimal activity as a monotherapy, with the most apparent benefit coming when combined with PD-(L)1 antibodies in PD-L1–positive patients. The company will also host an investor call on Monday, April 12. • Agenus (AGEN $2.89; Outperform) will provide an update from the ongoing trial evaluating the combination of AGEN1181, a next-generation CTLA-4 antibody with Fc enhancements, and balstilimab, the company’s PD-1 antibody. As of February, the company reported a 23% response rate (5/22 patients), achieving responses in tumors unlikely to respond to PD-(L)1 antibody monotherapy, including microsatellite stable colorectal and endometrial cancers. We will host a call with Agenus management on Saturday, April 10, to discuss the updated results (see page 5 for registration link). • Although mainly preclinical in nature, several companies will provide updates on KRAS G12C inhibitors, attempting to improve on the results presented to date by Amgen (AMGN $249.10; Market Perform) and Mirati (MRTX $173.91). In particular, the abstracts focus on proposed combination regimens, with preclinical efficacy reported for several combinations targeting the MAPK pathway.
Agenus Agenus will present updated clinical data with the company’s novel Fc-enhanced CTLA-4 antibody, AGEN1181, for which the company has previously disclosed multiple confirmed responses as monotherapy and in combination with the PD1 antibody balstilimab. As of the most recent update, the combination of AGEN1181 and balstilimab resulted in a 23% response rate (5/22) across a variety of tumor types, including many that would not be expected to respond to PD-(L)1 monotherapy, such as microsatellite stable (MSS) colorectal cancer (CRC) and MSS endometrial cancer. These particularly tough-to-treat cancer types do not respond to PD-(L)1 monotherapy, making the initial data for AGEN1181 combination more impressive. Two MSS endometrial cancer patients have achieved responses, one on monotherapy AGEN1181 and a second on the combination with balstilimab. In addition, a confirmed partial response in an MSS CRC patient treated with the combination was also announced in February of this year. We continue to be encouraged by the safety profile of the drug and initial biomarker and efficacy data, and look forward to additional updates at the upcoming AACR meeting
p
SunTrust just released a note stating that a series of strong data catalysts&disruptive medicines being commercialized or entering the clinic they recommend investors being overweight biotech. Their recommendations are:
$INCY Incyte Corporation: The Phase I/II trial (NCT02697591) evaluating open- label, dose-escalation, safety study of INCAGN01876 in subjects with Advanced or Metastatic Solid Tumors has completed patient recruitment.
Fellow Rigel shareholders: stay strong and stay patient. Despite the 350M upfront payment from Roche to Atea for a Phase 2 asset, a lot of promising biotechs were down today. $AGEN $BCRX (which has a potential oral treatment for Covid-19) $GTHX $INCY $BMRN $IMGN $CLVS $SGEN all down today. Have a nice weekend.
a
@andybiotech
A tougher FDA?🤔
At least 8 clinical holds in past 2wks $GILD Magrolimab $TGTX U2 combo $CRTX COR388 $MBIO MB-207 $VKTX VK0214 $YMTX YTX-7739 $DYN DYNE-251 $DNLI DNL919
2 BLA/NDA withdrawn due to non-alignment on PMS $REGN cemiplimab in 2L cervical $INCY parsaclisib in lymphoma
jacosa: Any comment on the twit posting i just read?
TheJ_stocktwits 3/1/22, 05:58 PM $CTIC $INCY Hmmm seems too obvious INCY should buy out CTIC. From the cc today: Gil Joseph Blum Needham & Company, LLC, Research Division – Analyst ... From what I remember, patients who go on drug eventually go on ruxolitinib (INCY Jakafi), eventually all progressed to being thrombocytopenic. How long does that usually take?
Jim Fong CTI BioPharma Corp. – SVP of US Commercial Operations Yes, Gil, typically, depending on the dose that they're on, when you look at the COMFORT trial, at their normal starting dose of 15 and 20 milligrams BID, you see about a 40% drop in platelet counts that occurs within the first 8 weeks. So it occurs pretty rapidly. Now as you go down in the doses, you start to see that taper off a bit. But again, you'll see that typically in the first 8 weeks of treatment.
@jbuell01 2h2 hours ago More Jennifer Buell Retweeted Agenus Inc. ($AGEN) .@FierceBiotech your @9:45AM report by Nick Paul Taylor is wrong. Correct deal terms below: $AGEN retains 67% of royalties & 90% milestones. Call with questions.Jennifer Buell added, Agenus Inc. ($AGEN)
@Agenus_Bio Received $15 M from $XOMA for minority royalty interest in $INCY, $MRK partnerships. $AGEN retain 67% of royalties and 90% of milestone payments; Remain eligible for up to an additional $450 M and $85.5 M in milestones from @Incyte and @Merck, respectively … 1 reply 6 retweets 6 likes Reply 1 Retweet 6 Like 6
Garo Armen
@garo_armen 3h3 hours ago More There will also be unscrupulous characters who intentionally say wrong or do wrong regardless of the facts.
@garo_armen 5h5 hours ago More Today’s announcement is the first and the smallest of multiple transactions we expect to conclude this year. Agenus Closes $15 Million Partial Royalty Monetization With XOMA
ORACLE INVESTMENT MANAGEMENT INC 13F doubles up on $AGEN shares , top buy in Q also $AGEN calls 2nd $PACB 3rd $OPK top $AGEN holders are $INCY and $GILD
even with news of a hope for baricitinib this stock goes down
$INCY Lancet Journal author submits findings from use of artificial intelligence to make recommendations for suggestions of compounds likely to be effective as potential CoronaVirus treatment. #baricitinib feb3
In a bigger picture, directly compare to JAKAFI $INCY in naive MF patients and show superiority in two major endpoints (SVR. TSS. ), better trends in Overall Survival. Potentially is the BEST jak inhibitor in every MF populations!
Andy Biotech: Except you forget I/O legend $INCY Epacadostat
$NKTR peg-IL2 vs $INCY IDO combo in 1L melanoma ORR: 53% (20/38) vs 65% (26/40) ORR in PD-L1+: 64% (14/22) vs 75% (9/12) ORR in PD-L1-: 39% (5/13) vs 56% (9/16) 12mo PFS: 57% vs 63%
A
Who’s next buyout coming AMRN and RDUS Buy who $GILD. $MRK. $INCY. $NVS
in case misery needs comapny
$KOD -93%
$BGNE -54%
$ACAD -30%
$SGEN -22%
$INCY +3%
The present disclosure provides #multispecific (e.g., bispecific) #antibodies that specifically bind to human GITR and/or human #OX40
$INCY partnered
Top takeout targets, per new Credit Suisse investor survey:
1. $CLVS
2. $SRPT
3. $ALDR
4. $INCY
5. $BMRN
6. $GLPG
7. $ALXN
8. $IMMU
9. $ICPT
10. $VKTX
On Saturday, April 10, through Thursday, April 15, the American Association of Cancer
Research (AACR) will host the first of two week-long virtual conferences, with the second to
be hosted on Monday, May 17, through Friday, May 21. Full regular abstracts were posted to
the AACR meeting website on March 10 with clinical trial and late-breaking abstracts to be
released at the start of the conference, and in this note we highlight several important data
presentations for our coverage list and other data of interest. In addition, an itinerary of all
relevant presentations to our coverage list and the wider oncology landscape is appended at
the end of this note.
In particular, we highlight:
• Incyte (INCY $83.18; Outperform) will be providing the first clinical update with the
company’s A2A/A2B receptor inhibitor and hosting a conference call with investors
(on Monday, April 12) to discuss the company’s broader adenosine targeting strategy,
including a CD73 antibody. The adenosine pathway has garnered significant industry
interest, and therapies targeting this pathway have led to monotherapy responses,
although clear clinical development paths have yet to be established, in our opinion.
• The next data point for TIGIT antibodies will come from iTeos (ITOS $34.54), which will
present preliminary Phase I data with EOS884448 as a monotherapy. Recent management
commentary suggests pharmacodynamic effects of EOS884448 will be focused on the
periphery for the AACR presentation, with biopsy analysis coming later in the year. Recall
other TIGIT antibodies have shown minimal activity as a monotherapy, with the most
apparent benefit coming when combined with PD-(L)1 antibodies in PD-L1–positive
patients. The company will also host an investor call on Monday, April 12.
• Agenus (AGEN $2.89; Outperform) will provide an update from the ongoing trial
evaluating the combination of AGEN1181, a next-generation CTLA-4 antibody with
Fc enhancements, and balstilimab, the company’s PD-1 antibody. As of February, the
company reported a 23% response rate (5/22 patients), achieving responses in tumors
unlikely to respond to PD-(L)1 antibody monotherapy, including microsatellite stable
colorectal and endometrial cancers. We will host a call with Agenus management on
Saturday, April 10, to discuss the updated results (see page 5 for registration link).
• Although mainly preclinical in nature, several companies will provide updates on KRAS
G12C inhibitors, attempting to improve on the results presented to date by Amgen
(AMGN $249.10; Market Perform) and Mirati (MRTX $173.91). In particular, the abstracts
focus on proposed combination regimens, with preclinical efficacy reported for several
combinations targeting the MAPK pathway.
Agenus
Agenus will present updated clinical data with the company’s novel Fc-enhanced CTLA-4 antibody, AGEN1181, for which the
company has previously disclosed multiple confirmed responses as monotherapy and in combination with the PD1 antibody
balstilimab. As of the most recent update, the combination of AGEN1181 and balstilimab resulted in a 23% response rate
(5/22) across a variety of tumor types, including many that would not be expected to respond to PD-(L)1 monotherapy, such
as microsatellite stable (MSS) colorectal cancer (CRC) and MSS endometrial cancer. These particularly tough-to-treat cancer
types do not respond to PD-(L)1 monotherapy, making the initial data for AGEN1181 combination more impressive. Two MSS
endometrial cancer patients have achieved responses, one on monotherapy AGEN1181 and a second on the combination with
balstilimab. In addition, a confirmed partial response in an MSS CRC patient treated with the combination was also announced
in February of this year. We continue to be encouraged by the safety profile of the drug and initial biomarker and efficacy data,
and look forward to additional updates at the upcoming AACR meeting
$CRSP $BMRN $CBAY
$EDIT $EXEL $INCY
$MRTX
$RARE $SAGE $SRPT $VKTX $WVE
Our time is coming - just be patient.
A tougher FDA?🤔
At least 8 clinical holds in past 2wks
$GILD Magrolimab
$TGTX U2 combo
$CRTX COR388
$MBIO MB-207
$VKTX VK0214
$YMTX YTX-7739
$DYN DYNE-251
$DNLI DNL919
2 BLA/NDA withdrawn due to non-alignment on PMS
$REGN cemiplimab in 2L cervical
$INCY parsaclisib in lymphoma
TheJ_stocktwits 3/1/22, 05:58 PM
$CTIC
$INCY
Hmmm seems too obvious INCY should buy out CTIC.
From the cc today:
Gil Joseph Blum Needham & Company, LLC, Research Division – Analyst
... From what I remember, patients who go on drug eventually go on ruxolitinib (INCY Jakafi), eventually all progressed to being thrombocytopenic. How long does that usually take?
Jim Fong CTI BioPharma Corp. – SVP of US Commercial Operations
Yes, Gil, typically, depending on the dose that they're on, when you look at the COMFORT trial, at their normal starting dose of 15 and 20 milligrams BID, you see about a 40% drop in platelet counts that occurs within the first 8 weeks. So it occurs pretty rapidly. Now as you go down in the doses, you start to see that taper off a bit. But again, you'll see that typically in the first 8 weeks of treatment.
$INCY The FDA granted Incyte's Parsaclisib orphan status for its treatment of splenic marginal zone lymphoma.
Jennifer Buell
@jbuell01
2h2 hours ago
More Jennifer Buell Retweeted Agenus Inc. ($AGEN)
.@FierceBiotech your @9:45AM report by Nick Paul Taylor is wrong. Correct deal terms below: $AGEN retains 67% of royalties & 90% milestones. Call with questions.Jennifer Buell added,
Agenus Inc. ($AGEN)
@Agenus_Bio
Received $15 M from $XOMA for minority royalty interest in $INCY, $MRK partnerships. $AGEN retain 67% of royalties and 90% of milestone payments; Remain eligible for up to an additional $450 M and $85.5 M in milestones from @Incyte and @Merck, respectively
…
1 reply 6 retweets 6 likes
Reply 1 Retweet 6 Like 6
Garo Armen
@garo_armen
3h3 hours ago
More
There will also be unscrupulous characters who intentionally say wrong or do wrong regardless of the facts.
0 replies 1 retweet 4 likes
Reply Retweet 1 Like 4
Garo Armen
@garo_armen
5h5 hours ago
More
Today’s announcement is the first and the smallest of multiple transactions we expect to conclude this year. Agenus Closes $15 Million Partial Royalty Monetization With XOMA
Potential top 5 acquirers: $CELG, $PFE, $GILD, $MRK, $JNJ ...expect the M&A focus to shift to ..: ( $AGIO (NDA filed), $CLVS, $EXEL, $INCY, $PBYI, $SGEN and $TSRO).
Great, then buy Agenus!
doubles up on $AGEN shares , top buy in Q
also $AGEN calls
2nd $PACB
3rd $OPK
top $AGEN holders are $INCY and $GILD
$INCY Lancet Journal author submits findings from use of artificial intelligence to make recommendations for suggestions of compounds likely to be effective as potential CoronaVirus treatment. #baricitinib feb3
$INCY
in naive MF patients and show superiority in two major endpoints (SVR. TSS. ), better trends in Overall Survival. Potentially is the BEST jak inhibitor in every MF populations!
$NKTR peg-IL2 vs $INCY IDO combo in 1L melanoma
ORR: 53% (20/38) vs 65% (26/40)
ORR in PD-L1+: 64% (14/22) vs 75% (9/12)
ORR in PD-L1-: 39% (5/13) vs 56% (9/16)
12mo PFS: 57% vs 63%
Incyte given $85.00 PT by Raymond James Financial. buy rating. http://www.marketbeat.com/r/1002538 $INCY