The independent financial analyst theScreener just lowered the general evaluation of CELLTRION INCORPORATED (KR), active in the Biotechnology industry. As regards its fundamental valuation, the title now shows 0 out of 4 stars while market behaviour can be considered moderately risky. theScreener believes that the title remains under pressure due to the loss of a star(s) and downgrades its general evaluation to Slightly Negative. As of the analysis date February 15, 2022, the closing price was K...
Hong Kong, China Begin To Participate We remain bullish and believe the path of least resistance is higher for global equities in the coming weeks and months. Where it gets difficult is in predicting near-term expectations due to the current overbought conditions based on indicators such as RSI and the percentage of MSCI ACWI stocks above their 50-day MAs. At this stage it is tough to get too excited for additional and significant near-term appreciation because of short-term overbought conditio...
Global Equities Stumbling Again We continue to believe global equities (ACWI-US) are likely to test the recent low made on March 23, with an undercut of roughly 10% also in the cards. This expectation is supported by price action during prior major waterfall declines in past recessionary periods. It is also worth noting that 15-25% rallies are to be expected within bear markets -- potentially multiple. During 2001-2002 the S&P 500 had two 20-25% rallies, and both ended up failing and breaking t...
INCHEON, Corée du Sud--(BUSINESS WIRE)-- Celltrion Healthcare annonce ce jour que le Comité des médicaments à usage humain (CHMP) de l'Agence européenne des médicaments (EMA) a adopté un avis favorable pour le CT-P13 SC en vue d'une autorisation de mise sur le marché dans l'Union européenne (UE) pour les personnes atteintes d'arthrite rhumatoïde (AR). Le CT-P13 SC est la version sous-cutanée du Remsima® (infliximab biosimilaire, CT-P13). Cette recommandation sera évaluée par la Commission européenne, l'organe compétent pour l'approbation des médicaments dans l'UE. Une formulation sous-cutan...
INCHEON, South Korea--(BUSINESS WIRE)-- Celltrion Healthcare today announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has adopted a positive opinion for CT-P13 SC for marketing authorisation in the European Union (EU) in people with rheumatoid arthritis (RA). CT-P13 SC is the subcutaneous version of Remsima® (biosimilar infliximab, CT-P13). This recommendation will now be reviewed by the European Commission, which has the authority to approve medicines in the EU. A subcutaneous formulation has the potential to enhance treatment opt...
- We maintain our BUY and our KRW360,000 target price on Celltrion in light of the likely US sales approval of Truxima and Herzuma in 2H18 and the long-term momentum to come from subcutaneous Remsima and Inflectra. - 1Q18 review: Results were in line with market expectations as the market share of Truxima, a rituxan biosimilar which made a European debut in 2017, expanded more rapidly compared with Remsima. Sales came in at KRW245bn (+25% YoY), operating profit at KRW116.5bn (...
VIENNA--(BUSINESS WIRE)-- Twelve-month data from the Personalised Anti-TNF therapy in Crohn’s disease Study (PANTS) was presented at the 13th Congress of the European Crohn’s and Colitis Organisation (ECCO). The results indicate that the clinical effectiveness, safety and immunogenicity of Celltrion Healthcare’s CT-P13 (biosimilar infliximab) in patients with Crohn’s disease (CD) is comparable to those treated with reference infliximab as well as those treated with adalimumab.1 The UK-wide, three-year prospective observationa...
VIENNE--(BUSINESS WIRE)-- Douze mois de données provenant de l’étude de thérapie anti-TNF personnalisée dans la maladie de Crohn (PANTS) ont été présentées lors du 13e congrès de l’Organisation Européenne de la Maladie de Crohn et de la Colite (ECCO). Les résultats indiquent que l’efficacité clinique, l’innocuité et l’immunogénicité du CT-P13 (infliximab biosimilaire) de Celltrion Healthcare sont similaires à celles d’un traitement avec l’infliximab de référence et l’adalimumab chez les patients atteints de la maladie de Crohn (MC).1 ...
INCHEON, South Korea--(BUSINESS WIRE)-- Celltrion, Inc. (KOSDAQ: 068270) announced today that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) issued a positive opinion recommending that Herzuma® (trastuzumab biosimilar) be granted marketing authorization in the European Union (EU) for the treatment of patients with early breast cancer, metastatic breast cancer, or metastatic gastric cancer whose tumors have either HER2 overexpression or HER2 gene amplification. The CHMP’s opinion...
Biologics to grow faster than traditional/chemical drugs Biologics are diversified into biological medicines (vaccines, blood components), genetically modified drugs (antibody drugs), cell therapy, gene therapy drugs, etc. These drugs require intensive R&D and costly production facilities, which naturally pose a high entry barrier. They have fewer side effects vs. chemical drugs and demonstrate great efficacy against certain diseases. They also grant a long patent protection per...
Ford Equity International Research Reports cover 60 countries with over 30,000 stocks traded on international exchanges. A proprietary quantitative system compares each company to its peers on proven measures of business value, growth characteristics, and investor behavior. Ford's three recommendation ratings buy, hold and sell, represent each stock’s return potential relative to its own country market.. The rating reports which are generated each week, include the fundamental details behind...
INCHEON, Corée du Sud--(BUSINESS WIRE)-- Celltrion Healthcare accueille avec joie la publication du récent énoncé de position de l’Organisation Européenne de la Maladie de Crohn et de la Colite (ECCO) sur l'utilisation des biosimilaires dans le cadre des maladies inflammatoires de l’intestin (MII). Un rapport qui encourage la transition du produit de référence infliximab vers l'infliximab biosimilaire.1 La déclaration d’ECCO couvre plusieurs aspects liés aux biosimilaires et présente ses positions clés :1 ...
INCHEON, South Korea--(BUSINESS WIRE)-- Celltrion Healthcare welcomes the publication of the latest position paper from the European Crohn’s and Colitis Organisation (ECCO) on the use of biosimilars for inflammatory bowel disease (IBD), which supports switching from reference infliximab to biosimilar infliximab.1 The ECCO statement covers several aspects related to biosimilars and the key positions are:1 Switching from the originator to a biosimilar in patients with IBD is acceptable following appropriate ...
SAN DIEGO--(BUSINESS WIRE)-- De nouveaux résultats présentés à l’occasion du congrès annuel 2016 de l’American Society of Hematology (ASH) démontrent que le CT-P10 (candidat biosimilaire du rituximab) et le rituximab de référence sont équivalents en termes de pharmacocinétique (PC) chez les patients atteints d’un lymphome folliculaire à un stade avancé (LFA), une forme de lymphome non-hodgkinien (LNH). 1 Au total, 121 patients souffrant de LFA ont été recrutés selon un ratio de 1:1 (59 patients pour le CT-P10 et 62 patients p...
SAN DIEGO--(BUSINESS WIRE)-- New data presented at the 2016 American Society of Hematology (ASH) Annual Meeting demonstrate that CT-P10 (biosimilar rituximab candidate) and reference rituximab are equivalent in terms of pharmacokinetics (PK) in patients with advanced follicular lymphoma (AFL), a form of non-Hodgkin lymphoma. 1 A total of 121 AFL patients were enrolled in a 1:1 ratio (59 patients on CT-P10 and 62 patients on reference rituximab) to demonstrate PK similarity of CT-P10 to reference rituximab, each given in combi...
WASHINGTON--(BUSINESS WIRE)-- Les nouvelles données présentées ce jour au congrès annuel de l’American College of Rheumatology (ACR) démontrent que le profil d’efficacité et d’innocuité du CT-P10 (rituximab biosimilaire) pour le traitement des patients atteints de polyarthrite rhumatoïde (PR) est comparable à celui des patients traités avec un rituximab princeps sur une période de 24 semaines.1,2 Un total de 372 patients atteints de PR (161 patients traités au CT-P10 et 211 patients au rituximab princeps) ont participé à un e...
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