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Analyst reports 2018

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avantiavanti
4
En daar komen de eerste reacties

Morgan Stanley 12 september 2018

FINCH2 Clean Across the Board

Efficacy is at least as good as other PhIII JAK data to date, with very clean safety and no cases of DVT/PE. While we await further details on Hb, platelets and overall infections, SAE rates were low. We expect GILD up low single digit % and GLPG up at least mid single digit %.

First PhIII dataset release for filgotinib: Gilead and Galapagos released top line data from FINCH2, the PhIII study of filgotinib in moderate-to-severe rheumatoid arthritis (RA) patients who have not responded or are intolerant to biologics. This is the first of the three FINCH RA studies to readout, and the first PhIII dataset for filgotinib. Both doses of filgotinib evaluated (100mg and 200mg) met the primary endpoint of ACR20 at week 12, and also demonstrated stat. sig. results on secondary endpoints ACR50, ACR70, DAS28 (CRP) = 3.2 (low disease activity), and DAS28 (CRP) = 2.6 (clinical remission) at weeks 12 and 24. SAEs occurred in 3.4%, 5.2%, and 4.1% of patients treated with placebo, 100mg filgotinib, and 200mg filgotinib, respectively, with no cases of DVT or PE reported. There were two cases of uncomplicated herpes zoster in each filgotinib group, one case of myocardial ischemia observed in the 100mg filgotinib group, and one case of non-serious retinal vein occlusion in the 200mg filgotinib group. A comparison of the FINCH2 dataset to prior JAK RA datasets is provided below.

Clean start to FINCH data: While cross trial comparisons are challenging given the underlying differences in patient populations and trial design, we believe the FINCH2 efficacy data appears at least as good as upadacitinib efficacy in biological nonresponders (AbbVie is covered by David Risinger). Investors were also focused on any new cases of DVT/PE, especially following the PhII TORTUGA top line release last week (see our note here) in which there was one case of VTE deemed unrelated to treatment, and we see the lack of DVT/PE in FINCH2 as highly encouraging. We await more detailed data, especially to learn more about the infections observed in each filgotinib group, hemoglobin, and to better understand baseline characteristics, but the data is clean and bodes well for filgotinib into the FINCH1 and FINCH3 readouts in early 2019. We expect GILD up low single digit % and GLPG up at least mid single digit % on the news.
avantiavanti
5

Barclays 12 september 2018

Gilead Sciences

Thoughts on the filgotinib FINCH2 RA data

Stock Rating/Industry View: Overweight/Positive
Price Target: USD 90.00
Price (11-Sep-2018): USD 72.23
Potential Upside/Downside: 25%
Tickers: GILD

Efficacy data in-line, positive safety profile potentially offers differentiation. We look for modest strength in GILD shares tomorrow morning following the announcement of positive top-line data from FINCH2, the first phase 3 of filgotinib—partnered with Galapagos (covered by EU Pharma analyst Emily Field; OW/Pos, €130 PT)—in rheumatoid arthritis (RA). That the efficacy outcomes are positive—FINCH2 hit on the primary and all key secondary endpoints—isn’t much of surprise given the strong phase 2 data in RA (DARWIN1 and 2) and other indications (UC, Crohn’s, psoriatic arthritis). Moreover the oral JAK inhibitors (JAKis) class for RA has become increasingly de-risked following the approval of Pfizer’s Xeljanz (2017 sales: $1.3B) and Lilly/Incyte’s Olumiant and AbbVie’s comprehensive upadacitinib’s positive phase 3 outcomes (see ABBV - Thoughts on the SELECT-COMPARE data, 04/09/18)—and we note the generally comparable efficacy outcomes of FINCH2 vs. other phase 3s in patients with inadequate responses to biologics (Figure 2). However given that safety/ tolerability concerns of the JAKis delayed the approval of Xeljanz in Europe and Olumiant in the US (see LLY/INCY - FDA approves 2mg Olumiant dose with black box warning, 06/01/18), we see potential differentiation of filgotinib’s safety profile—likely attributable to its relatively high specificity for JAK1 (Figure 1) leading to fewer off-target interactions—allowing for meaningful penetration in what looks to be an increasingly crowded market.

Filgotinib bolsters near-term growth outlook; filing remains likely 1H20. Although filgotinib is not a significant contributor to our positive thesis on Gilead, offering incremental upside relative to HIV near-term and the CAR-T portfolio longer-term—we forecast initial sales in 2020 of $134M (cons: $168M) growing to $650M in 2022 (cons: $775M)—it remains a part of an attractive pipeline (including NASH), reinforcing our outlook for growth starting 2019 following a 2018 trough. Looking ahead, read-outs for the remaining phase 3 RA studies FINCH-1 (methotrexate-inadequate responders) and FINCH-3 (methotrexate-naïve) are expected 1H19, which together with additional safety data—including from the male toxicity study MANTA—which remains the rate-limiting step, should support a regulatory submission possibly late 2019 but more likely 1H20 (see GILD - Thoughts on the filgotinib potential regulatory timeline, 08/03/18). Maintaining OW and $90 PT for Gilead.

FINCH2 overview and efficacy data. FINCH2 was a randomized, placebo-controlled study evaluating two doses QD (100mg and 200mg) of filgotinib in N=448 RA patients with an inadequate response to biologic disease-modifying anti-rheumatic drug(s) (bDMARDs) on a background of conventional synthetic DMARDs. The study met its primary endpoint, proportion of those achieving an ACR20 improvement, with 57.5% at 100mg QD (p=<0.001) and 66.0% at 200mg (p=<0.001) vs. 31.1% of placebo at 12 weeks. Other key secondary endpoints were also met including: ACR50, ACR70, low disease activity (defined as DAS28(CRP)=3.2), and clinical remission (DAS28(CRP)<2.6) (see Figure 2 for a cross-trial comparison).

FINCH2 safety data No new safety signals were observed in the study, with most TEAEs and SAEs described as mild-to-moderate. Discontinuations due to TEAEs were not disclosed but reported to be similar across the arms. There were two cses of herpes zoster in each filgotinib arm; two cardiovascular events were also observed, one in the placebo arm and one in the filgotinib 100mg arm. There was also one case of non-serious retinal vein occlusion in the 200mg treatment arm, but no incidences of deep venous thrombosis, pulmonary embolism, opportunistic infections, malignancies, or deaths in the study.
avantiavanti
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Kempen 12 september 2018

Galapagos - Filgotinib hits the JAKpot

FINCH 2 with filgotinib in TNF-IR patients showed the best results we could hope for, meeting all primary and secondary endpoints with highly stat sig differences. Notably, the placebo-adjusted scores come on top of the precedent range for JAKs and at least as good as AbbVie’s upadacitinib in TNF-IR. Equally important, the safety profile is unquestionably clean and better than any other JAKs or biologics with no incidence of DVT/PE and only 2 herpes events per dose arm. While the outstanding profile should be confirmed in the larger FINCH 1 and FINCH 3 trials (expected by Q1’19), the FINCH 2 results clearly demonstrate that filgotinib is not the last but the first JAK in line, deserving premium market share. We increase our market share assumption in the TNF-IR population to 35% and as a result, our PT goes to €125 (from €115). We reiterate our BUY and Galapagos continues to feature on our favorites list.
avantiavanti
7
DeGroof Petercam 12 september 2018

Galapagos (Buy) - Competitive FINCH-2 data (EUR 89 / TP EUR 125 from 110)

Facts – Study reaches all primary and key secondary efficacy endpoints


The Phase III study (FINCH-2) evaluating filgotinib in patients with moderately-to-severe active rheumatoid arthritis and prior inadequate response/intolerance to biologic agents achieved its primary endpoint in the proportion of patients achieving an American College of Rheumatology 20 percent (ACR20) response at Week 12.
Also at Weeks 12 and 24, the proportion of patients achieving ACR50 and ACR70, low disease activity (LDA, DAS28(CRP) = 3.2), and clinical remission (DAS28(CRP) < 2.6) were significantly higher for patients receiving once-daily filgotinib 100 mg or 200 mg compared to patients receiving placebo.

No new safety signals were reported compared to those reported in previous filgotinib trials. Serious adverse events occurred in 3.4, 5.2 and 4.1 percent of the patients in the placebo, 100mg and 200mg groups, respectively.
There were two cases of uncomplicated herpes zoster reported in each filgotinib group and two major adverse cardiovascular events (MACE) were identified, one in the placebo group and one in the filgotinib 100 mg group.
There was one case of non-serious retinal vein occlusion in the filgotinib 200 mg group and no reports of deep venous thrombosis (DVT) or pulmonary embolism (PE). There were no deaths, malignancies, gastrointestinal perforations, or opportunistic infections, including active tuberculosis.

Our view – Competitive results, continuing to show good safety profile
Efficacy results are competitive compared to other JAKs (tofacitinib, baricitinib and upadacitinib; see graphs in attachment) and the safety profile remains strong, although we do not have the complete data set at this time.
The patients included in the FINCH-2 trial were irresponsive or intolerant to biologic therapies and are thus the most difficult to treat population. As such, these results further derisk the large FINCH-1 and FINCH-3 RA studies for which we expect results early 2019.
The main safety item to watch in this class of therapies is the occurrence of deep vein thromboses (DVT) and infections. Questions on DVTs caused significant delays in the marketing approval of baricitinib (Olumiant). No incidences of DVT were reported in FINCH-2. While there were two incidences of heart failure, one of these events were noticed in the placebo group, indicating there is no imbalance. Furthermore, filgotinib keeps on reporting a very low number of herpes zoster cases.

Two JAK inhibitors have received marketing approval to date, Xeljanz (Pfizer) and more recently Olumiant (Eli Lilly). The safety profile of these molecules has been severely scrutinized, yet Pfizer was able to report over EUR 1.3bn in sales for Xeljanz in 2017 and Olumiant showed the most successful launch to date in rheumatoid arthritis. In our view, filgotinib and AbbVie’s upadacitinib will dominate the market once they receive regulatory approval. These JAK inhibitors are designed to be more selective for JAK1 and are consequently expected to present an improved safety profile. To date, filgotinib seems to display the best safety profile.

Investment conclusion

This strong set of results demonstrates the competiveness of Gilead and Galapagos’ JAK inhibitor and warrants further upwards revisions in our model. Based on the reported safety profile of filgotinib, an increased probability of success for the complete RA program (from 75% to 85%) and the potential to expand the use of filgotinib towards multiple indications, we preliminary increase our TP to EUR 125 from 110.

The strong results might also rejuvenate rumors on a potential take-over by Gilead. Remember that Galapagos will be eligible to receive royalties in the 20%-30% range as well commercial milestones (> USD 1bn) from Gilead. With a potential blockbuster drug in hand, we figure that the financials for Gilead would make more sense in an M&A-approach.
Galapagos was and continues to be our preferred play in our space, we stick to our Buy rating.
avantiavanti
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Berenberg

Date: Wed, 12 Sep 2018 07:43:34 +0000
Subject: Galapagos (GLPG NA) - Filgotinib clears major hurdle with FINCH 2
Galapagos (GLPG NA, Buy; PT EUR 112.00)

Galapagos has announced positive data from its phase III trial FINCH 2, which evaluated filgotinib in patients with rheumatoid arthritis (RA) with an inadequate response to biologic agents, effectively the third line setting. This is the first phase III trial to read out from the programme and marks a big milestone in Galapagos’s pipeline for its most advanced drug, as an approval and good competitive position within the class is increasingly within reach. Filgotinib is in a class of drugs called JAK inhibitors which includes Pfizer’s Xeljanz, Eli Lilly’s Olumiant and Abbvie’s upadacitinib (approval expected in 2019).

In FINCH 2, two doses (100mg and 200mg) of filgotinib were compared to placebo in 449 patients over 24 weeks. The primary end-point was the proportion of patients who achieved an 20% improvement in ACR response (ACR20) at week 12, and key secondary end-points included ACR20 at 24 weeks as well as ACR50 and ACR70 at both 12 and 24 weeks. FINCH 2 met its primary and all key secondary end-points. Reassuringly, there was a clear dose response, with the high dose demonstrating greater efficacy than the low dose – something that has not been consistently seen with competitor agents. See enclosed table for efficacy data compared to Xeljanz and upadacitinib in comparable trials.

While the efficacy results are certainly reassuring, the key differentiation was always going to be safety/toxicity. No new safety signals were seen in the trial. Importantly, there were no deaths, malignancies, opportunistic infections, pulmonary embolism or DVTs – which have been seen with competitor drugs. Cardiovascular events were balanced between the placebo and drug arms. There was one case of retinal vein occlusion (a blood clot near the eye) in a patient who received 200mg filgotinib which was considered to be non-serious. Overall, these safety data set it apart from its competition, importantly from Abbvie’s upadacitinib, which reported two deaths and two cases of pulmonary embolism in the comparable trial SELECT-BEYOND. Filgotinib is increasingly looking like a best-in-class agent.

We forecast peak sales of USD4bn (EUR3.5bn), which assumes success in RA across all lines of therapy as well as inflammatory bowel disease, risk adjusted to 75%, as we await these further data. For Gilead, which will market the drug and pay a royalty and milestones to Galapagos, the news is also a positive. By mid-2019, we expect data from the ongoing FINCH 1 and FINCH 3 trials which are evaluating filgotinib in the second line (compared to Humira) and first line (compared to methotrexate) settings. There are also ongoing phase III trials in Crohn’s disease (DIVERSITY) and Ulcerative colitis (SELECTION), which are both expected to complete in late 2019.

Our valuation is based on a SOTP of the pipeline, with filgotinib comprising 45% of the whole company NPV
avantiavanti
5


Goldman Sachs Research


Galapagos NV (GLPG.AS): Positive Phase 3 data for Filgotinib in rheumatoid arthritis clears first hurdle


Yesterday after market close Galapagos and partner Gilead (covered by Terence Flynn) reported positive topline data from the first Phase 3 trial (FINCH2) for filgotinib (JAK inhibitor) for the treatment of rheumatoid arthritis (RA). Despite the caveat of cross trial comparisons, we view the efficacy data to be broadly comparable with those from Abbvie’s upadacitinib and there was nothing that was overly concerning from a safety perspective - the latter being a major point of focus for investors. For Galapagos, filgotinib is its key pipeline asset and c.75% of our €96 12m price target can be associated to fligotinib linked milestones and royalties across various indications. For RA in particular, we currently forecast unadjusted, in-market sales of c.$2.4bn in 2030. We apply a 70% risk adjustment to these revenues and have assumed that Galapagos receives c.€480 mn in profits/royalties. Based on our DCF-based valuation (which forms the basis of the fundamental valuation for our 12-month price target), filgotinib in RA (ie. royalties and milestone payments but excluding corporate costs) is worth €38 per share of our €96 12m price target (40% of NPV). The next key catalysts for filgotinib are the two Phase 3 (FINCH 3 and 1) data in RA which are expected in 1H19.

Results details: The FINCH2 study was evaluating the efficacy and safety of filgotinib (100mg or 200mg) in adult patients with moderate-to-severe rheumatoid arthritis who had not adequately responded to biologic anti-rheumatic drugs (DMARDs). The primary endpoint of the study was the proportion of patients achieving an ACR20 response at week 12. Filgotinib demonstrated an ACR20 at week 12 of 57.5%/66.0% for the 100mg/200mg arm, respectively, compared to placebo 31.1% (p<0.001), achieving the primary endpoint (Exhibit 1). In addition, both doses of filgotinib achieved all key secondary efficacy endpoints, including low disease activity and clinical remission. Despite limitations of cross trial comparisons, for context, Abbvie's updacitinib demonstrated ACR20 of 65%/56% for 15mg/30mg vs. placebo 28% at week 12 in its Phase 3 (SELECT-BEYOND) study which enrolled patients that had an inadequate response to at least one biologic DMARD.

In terms of the safety/tolerability profile which was a major point of focus for investors (given prior safety concerns for the JAK class), filgotinib was generally well-tolerated with no safety signals which were overly concerning. Treatment-emergent/serious adverse events were mostly mild-to-moderate in severity, with serious adverse events reported in 5.2%/4.1%/3.4% patients receiving filgotinib 100mg/filgotinib 200mg/placebo. 2 cases of uncomplicated herpes zoster were reported in each filgotinib group. Two major adverse cardiovascular events were reported, one myocardial ischemia in the filgotinib 100mg arm and one subarachnoid hemorrhage in the placebo group, but encouragingly there were no reports of deep venous thrombosis or pulmonary embolism. One case of non-serious retinal vein occlusion was also reported in the filgotinib 200mg group, but there were no reports of deaths, malignancies, gastrointestinal perforations or opportunistic infections in any of the groups.

We are Neutral rated on Galapagos: Our 12-month price target of €96 is derived using a SOTP DCF-based value of €91/share (85% weighting) and an M&A valuation of €119/share (15% weighting). Our M&A valuation is calculated by: (1) applying a 7.5% WACC to our stand-alone DCF (assumed WACC of a larger potential acquirer); and (2) assuming 90% cost synergies. Upside risks: (1) superior efficacy/cleaner safety data for filgotinib vs. JAK class of inhibitors (2) trial success of IPF assets; Downside risks: (1) negative clinical trial outcome from the filgotinib trials (2) ability to recruit patients in the IPF trials (3) any announcement on partnership discontinuation.
avantiavanti
4
KBC

Galapagos - Filgo FINCH2 phIII in RA: positive on all fronts

News: Galapagos and Gilead communicated this morning on the long anticipated phase III results on filgotinib from the FINCH2 study in rheumatoid arthritis (RA).

FINCH2=a placebo-controlled phase III trial testing filgotinib (placebo (148 patients), 100mg (153 patients) and 200mg (147 patients), 1x/day oral admin) in adults with moderately-to-severe RA and prior inadequate response to other drugs (DMARDs).

Efficacy results:
1e endpoint=proportion of patients achieving the ACR20 score was achieved with significance at
a) week12 (placebo 31.1% vs filgo 100mg 57.5% and 200mg 66.0%) (p<0.001)
b) week24 (placebo 34.5% vs filgo 100mg 54.9% and 200mg 69.4%) (p<0.001)
Important to note is that for both doses – 100mg or 200mg filgo – and at the deeper response rate scorings – ACR50, ACR70 – as well as the Low Disease Activity (LDA) and Clinical remission score filgo scored with statistical significant response rates compared to placebo at w12 and w24.

Safety and tolerability results:
-treatment-emergent adverse (TEA) (placebo 3.4% vs 100mg 5.2% and 200mg 4.1%) and serious adverse events (SAE) were considered mild or moderate.
-uncomplicated Herpes zoster: 2 patients in both filgo 100mg and 200mg
-major adverse cardiovascular events (MACE): 1 patient in placebo, 1 patient in filgo 100mg
-retinal vein occlusion (non-serious): 1 patient in filgo 200mg
No reports of deep venous thrombosis (DVT) or pulmonary embolism (PE)
No deaths, GI perforations, opportunistic infections … raising concerns

Our View/Conclusion: As anticipated, the RA filgo dataset has been communicated to us before end of 3Q18 and brings positive datasets on all fronts with to date no major safety or tolerability concerns. With respect to response rate and deepness, we see comparable data to the other JAK inhibitors in the space (eg Upadacitnib from AbbVie) and a good safety profile which brings us good hope for the remainder of the upcoming phIII RA trials being FINCH3 (1,252 patients in total), FINCH1 (1,759 patients) with topline results anticipated for 1H19. As previously communicated by Gilead/Galapagos, the RA dataset can only be submitted together with the pending ongoing testicular (sperm) safety study MANTA for which timing of initial results cannot be defined yet.
Overall, 2019 will be a year rich in newsflow for GLPG with a series of filgo readouts from phIII and phII trials. With the news of today on RA, the tone has been set with high expectations for the Crohn’s/UC clinical trials. If there are no hickups, phIII topline results for UC (SELECTION1) and Crohn’s (DIVERSITY1) are on the schedule for 1H20.
We reiterate our Buy rating and maintain our TP at € 113.0/share (unchanged).
[verwijderd]
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Sommige analyses zijn van betere kwaliteit dan andere, en dan druk ik me zachtjes uit, maar overal voor bedankt, avanti.
avantiavanti
0
quote:

asti schreef op 12 september 2018 12:12:

Sommige analyses zijn van betere kwaliteit dan andere, en dan druk ik me zachtjes uit, maar overal voor bedankt, avanti.
Dat is absoluut zo Asti. Ik laat het hier ook bij, tenzij ik nog een opvallende of goeie voorbij zie komen.
Bolknak_26F5
0
(ABM FN-Dow Jones) Het extra kapitaal dat Galapagos vannacht heeft opgehaald, verschaft het biotechbedrijf extra ruimte om de testen voor het IPF-programma uit te voeren. Dat stellen analisten van KBC Securities donderdag.
Galapagos haalde afgelopen nacht met succes 300 miljoen dollar op bij Amerikaanse beleggers. Er werden 2.575.107 nieuwe gewone aandelen in de vorm van American Depositary Shares verkocht. Dit gebeurde tegen een prijs van 116,50 dollar.
Bij de publicatie van de halfjaarcijfers meldde Galapagos dat het 1,1 miljard euro in kas heeft.
Volgens de analisten van KBC is Galapagos door het extra kapitaal goed gepositioneerd bij klinische IPF testen in een latere fase. IPF is een chronische, onomkeerbaar progressieve fibrotische afwijking in de longen, die vooral voorkomt bij volwassenen boven de 40 jaar.
KBC Securities hanteert voor Galapagos een koopadvies met een koersdoel van 113,00 euro.
Het aandeel Galapagos verloor donderdag 1,4 procent op 103,05 euro.
Door: ABM Financial News.
maxen
5
Analist O. v.d. S. van Gala Securities over een eventuele overname:

"Dit is pas de eerste van drie fase III studies die we met filgotinib aan het doen zijn. Dus wat dat betreft
als Gilead al gedachten zou hebben zou het logischer zijn om eerst die andere fase III studies af te wachten. Wat hun plannen zijn weet ik niet. Dat overleggen ze ook niet met mij. Ik hoop alleen dat ze afstand bewaren."

kanaalz.knack.be/nieuws/galapagos-hee...

avantiavanti
8
JP Morgan 13 september 2018

JAK and the giant opportunity - Initiating at OW with a €120 Jun-19 PT c.15% upside potential

deel 1

Bijlage:
avantiavanti
6



DeGroof Petercam 24 september 2018

Galapagos (Buy) -Initiation of global Phase II trial with GLPG1972 in osteoarthritis (EUR 97 / TP EUR 125)

Facts – First dosing triggers EUR 9m milestone payment

Galapagos and partner Servier dosed the first patient in their global Phase II trial (ROCELLA) with GLPG1972 in knee osteoarthritis (OA) patients, triggering a EUR 9m milestone payment.
ROCCELLA is a multiregional, randomized, double-blind, placebo-controlled, dose ranging trial evaluating the efficacy and safety at week 52 of three different once-daily doses of GLPG1972 in patients with OA. ROCCELLA is planned to recruit approximately 850 patients in up to 15 countries.

The primary objective is to demonstrate the efficacy of at least one dose per day of GLPG1972 compared to placebo in reducing cartilage loss after 52 weeks of treatment. This cartilage loss will be measured precisely by magnetic resonance imaging (MRI). Secondary objectives include safety and tolerability, several additional measures of structural progression, improvement in pain, function, stiffness, and patient global assessment.
Galapagos will be responsible for ROCCELLA in the United States, where 300 patients are targeted to be recruited. Servier will run the trial in all other countries.

Our view - Targeting a large underserved market
OA is the most common joint disorder, with an estimated global prevalence of 8.2%. Pharmacological treatments are mainly related to relief of symptoms and there is no disease-modifying OA drug (treatment that will reduce symptoms in addition to slowing or stopping the disease progression) yet approved by the regulatory agencies.
GLPG1972 has previously shown a positive safety and tolerability profile in healthy volunteers and demonstrated a strong, dose-dependent reduction of a biomarker of cartilage breakdown. With only biomarker data available and a limited number of patients treated, the compound currently represents EUR 4 of our EUR 125 target price, but can become a valuable asset in this large underserved market once efficacy data in these OA patients demonstrate the potential to effectively modify the course of the disease.

Investment conclusion
The main focus point this year and into 2019 will be Galapagos and Gilead’s JAK inhibitor, filgotinib. The first Phase III trial in rheumatoid arthritis showed positive topline results and the market is awaiting the full data set (conference 4Q18) as well as confirmation of the safety and efficacy profile from the larger FINCH-1 and 3 studies (1H19). Furthermore, Galapagos continues to demonstrate the strength of its technology platform through the progress of its programs in idiopathic pulmonary fibrosis, atopic dermatitis and osteoarthritis. We reiterate our Buy recommendation.


Analyst: Stephanie Put, PhD
avantiavanti
3
GLPG/GILD: Filg ACR Abstract Just Posted; Supports Competitive Efficacy and Safety

October 4, 2018

RBC Capital Markets, LLC
Brian Abrahams (Analyst)

The late-breaker abstract for the ph.III FINCH 2 study for filgotinib in TNF-refractory RA was posted very recently, we believe just today, and contains several notable updates. Baseline characteristics show that the pts are comparable to the ph.III upadacitinib trial in TNF-refractory RA, allowing for meaningful comparisons to this key competitor be made. Additional efficacy measures and subgroup analyses support its potentially competitive efficacy profile and continue to suggest safety is as good as or better than upadacitinib. MANTA tox study remains key gating factor for filing but we believe today's updates are incrementally positive.


Baseline characteristics are very similar in FINCH 2 and SELECT-BEYOND suggesting head-to-head comparisons can be made to judge filgotinib's competitiveness to ABBV's Jak1 upadacitinib. The patients match up almost exactly in terms of age, years of RA duration, baseline number of tender and swollen joints and DAS28(CRP) - which should make it easier to compare the data, vs. the previous ph.IIs which had differing baseline characteristics.

New efficacy data are supportive of a competitive profile for filgotinib in this population. Several new measures of efficacy were reported in the abstract including HAQ-DI mean and change from baseline, SF-36 PCS and FACIT-Fatigue changes. From these the one comparison to upadacitinib that is possible to make (HAQ-DI CFB) based on the available data from the SELECT-BEYOND trial shows that filgotnib's placebo-adjusted efficacy is comparable (100mg: 0.25 vs. 0.22 for upa 15mg) or better (200mg: 0.32 vs. 0.24 for upa 30mg) than upadacitinib. This adds support to the competitiveness of the agent including at the lower 100mg dose, which had looked numerically inferior to upa on the previously-reported measures.

Safety continues to stack up well. We continue to see safety as a key gating factor and potentially a differentiator if additional ph.III filgotinib data continues to show a comparatively clean profile. Additional data in the abstract show that while there were slightly more AE-related discontinuations for filgotinib (3.4% and 3.9% for filgotinib groups vs. 2.0% for placebo), this was well within the range of noise relative to the upa study, and other parameters like OIs and malignancies, consistent with prior reports, look lower vs. for upa. Detailed lab changes were not reported in the abstract and we would look for this at the meeting. Curiously, the one case of retinal vein occlusion was classified under "DVT/PE" - suggesting the companies may view it as a thromboembolic event despite a description as "non-serious," which had led us to believe it was due to non-ischemic neovascularization/edema rather than thrombosis, but regardless the TE rate still looks lower vs. for upa.
avantiavanti
11
Bryan, Garnier & Co 2 oktober

Galapagos BUY Fair Value EUR120 Share price EUR96.26 Bloomberg / Reuters GLPG BB/GLPG.BR Healthcare Biotech

Slashed Price for a De-risked Blockbuster and Rich Pipeline!
Bijlage:
winx09
0
quote:

avantiavanti schreef op 8 oktober 2018 09:27:

Bryan, Garnier & Co 2 oktober

Galapagos BUY Fair Value EUR120 Share price EUR96.26 Bloomberg / Reuters GLPG BB/GLPG.BR Healthcare Biotech

Slashed Price for a De-risked Blockbuster and Rich Pipeline!
Weer bedankt Avantiavanti. Bryan, Garnier en Co bedoelt E96 met de "slashed price". Ondertussen is er al weer 10% van af.
Wellicht moeten we tot de Filgo Adcom wachten (1h20 ?) totdat de markt de waarde echt gaat inprijzen...

Keynes: The Market Can Remain Irrational Longer Than You Can Remain Solvent.
avantiavanti
6
Samenvatting van update Morgan Stanley 24 oktober 2018

Clean FINCH2 Data at ACR

Galapagos/Gilead presented detailed FINCH2 data for filgotinib in RA at ACR. Investors were most interested in safety, where we believe filgotinib demonstrated a clean profile, particularly on hemoglobin and platelet counts.

Galapagos/Gilead presented detailed FINCH2 data through a late breaking poster at the 2018 American College of Rheumatology/Association of Rheumatology Health Professionals (ACR/ARHP) Annual Meeting. Recall that positive top line data was released in September (see our take here), and we believe the detail presented further suggests a differentiated profile for filgotinib in RA. Efficacy highlights include a rapid onset of action, with both 100mg and 200mg filgotinib demonstrating stat. sig. ACR20 separation vs. placebo from two weeks onwards, and consistent, stat. sig. ACR20 responses for both doses of filgotinib across numerous subsets of prior biologic use. However, we believe investors were focused on safety, where we were most interested in changes in platelets and hemoglobin. Median values for both lab parameters were stable and in line with placebo throughout the study, with no clinically relevant changes reported. Additional safety parameters reported, including ALT and AST changes, also indicate filgotinib demonstrated a clean safety profile in FINCH2. There were no cases of DVT or PE reported. We await the whole of the FINCH program (FINCH1/3) in 2019 and look for more details at Galapagos' 2018 R&D Day on 10/25.
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Vertraagd 18 apr 2024 16:50
Koers 27,060
Verschil -0,320 (-1,17%)
Hoog 27,300
Laag 26,940
Volume 85.697
Volume gemiddeld 80.458
Volume gisteren 104.556

EU stocks, real time, by Cboe Europe Ltd.; Other, Euronext & US stocks by NYSE & Cboe BZX Exchange, 15 min. delayed
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