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Chi-Med Highlights Surufatinib Phase III Results in Neuroendocrine Tumors at ESMO 2020 and Publications in The Lancet Oncology

…complement previously presented positive Phase III SANET-ep results in patients with non-pancreatic NET, including across multiple subgroups ―   ― Results of both SANET-p and SANET-ep studies published in The…


Chi-Med Initiates Rolling Submission of NDA to U.S. FDA for Surufatinib for the Treatment of Advanced Neuroendocrine Tumors

…by 67%, extending PFS of non-pancreatic NET patients with an acceptable risk/benefit ratio – – The pivotal Phase III SANET-p trial demonstrated surufatinib reduced risk of progression or death by…


Chi-Med Reports Final Results for the Year Ended December 31, 2017 and Updates Shareholders on Key Clinical Programs

…line with guidance Group revenue up 12% to $241.2 million (2016: $216.1m); Net loss attributable to Chi-Med $26.7 million (2016: Net profit $11.7m), including $88.0 million in research and development…


Chi-Med Presented Sulfatinib Neuroendocrine Tumors Phase Ib/II Results at the 14th Annual Conference of the European Neuroendocrine Tumor Society

…and immune evasion. Five other sulfatinib clinical trials are underway in China and the U.S., including two Phase III studies in NET patients (SANET-p and SANET-ep), one Phase II study…


Chi-Med Reports 2017 Interim Results and Updates Shareholders on Key Clinical Programs

…$126.6 million (H1 2016: $104.5m). Net income attributable to Chi-Med of $1.7 million (H1 2016: $0.5m), including $37.5 million in research and development expenses on an as adjusted basis (H1…


Chi-Med Reports 2020 Interim Results and Provides Updates on Key Clinical Programs

…in May 2020 and subsequent grant of Priority Review status in July 2020. Surufatinib – Two NDAs with first China launch in NET planned for late 2020: Progressed non-pancreatic NET


Chi-Med Announces Second NDA Acceptance in China for Surufatinib in Pancreatic Neuroendocrine Tumors

…Society for Medical Oncology Congress (“ESMO”) (Abstract Number 1156O). This is the second NDA acceptance for surufatinib. The first NDA for non-pancreatic NET was accepted by the NMPA in November…


Chi-Med Reports Final Results for the Year Ended December 31, 2016 and Updates on Key Clinical Programs

…Hutchison China MediTech Limited (“Chi-Med”) Reports Final Results for the Year Ended December 31 , 2016 and Updates Shareholders on Key Clinical Programs Group: Record revenue, net income and…


Chi-Med Reports 2018 Full Year Results and Provides Updates on Key Clinical Programs

…(2017: $241.2m). N et loss attributable to Chi‑Med of $74.8 million (2017: net loss $26.7m). Adjusted Group net cash flow (non-GAAP) was -$57.3 million in 2018. Cash from our Commercial…


Chi-Med Reports 2019 Full Year Results and Provides Updates on Key Clinical Programs

…another two NDA3 submissions are imminent, one with savolitinib in lung cancer and a second with surufatinib in pancreatic NET, with launches anticipated for 2021.” “Based on extensive clinical data,…


Chi-Med Reports 2019 Interim Results and Provides Updates on Key Clinical Programs

…Chairman, Chi-Med. “All major clinical readouts in the first half were encouraging, with the stand-out results being surufatinib’s positive Phase III outcome in non-pancreatic NET and savolitinib’s preliminary data in…


Final Results for the year ended 31 December 2015

…104% to $178.2 million (2014: $87.3m). Net profit from operations attributable to Chi-Med of $8.0 million (2014: net loss -$7.3m), including our booking of $3.1 million in one-time preparation costs…


Chi-Med Plans to Submit Marketing Authorization Application for Surufatinib Following Scientific Advice from EMA’s CHMP

…that the completed SANET-ep (non-pancreatic NET) and SANET-p (pancreatic NET) studies, along with existing data from surufatinib in U.S. non-pancreatic and pancreatic NET patients, could form the basis to support…


Chi-Med initiates sulfatinib U.S. clinical trials

…tumours. A U.S. Phase II study in NET is expected to be initiated based on the conclusion of this Phase I dose escalation study. Sulfatinib is an oral drug candidate…


Chi-Med Plans to Submit NDA for Surufatinib Following Pre-NDA Meeting with the U.S. FDA

…SANET-p (pancreatic NET) studies, along with existing data from surufatinib in U.S. non-pancreatic and pancreatic NET patients, could form the basis to support a U.S. NDA submission. The FDA granted…


Chi-Med Reports Interim Results for the Six Months Ended June 30, 2016, Provides 2016 Financial Guidance and Updates Shareholders on Key Clinical Programs

…to $ 8 2 .3 million ( H1 201 5: $55.6m); Total sales of non-consolidated joint ventures up 9% to $249.6 million (H1 2015: $229.8m); Total net income attributable to…


Chi-Med Initiates a Phase II Trial of Surufatinib in Combination with Tuoyi in Patients with Advanced Solid Tumors

NET was accepted for review by the NMPA, and the U.S. Food and Drug Administration granted Orphan Drug designation to surufatinib for the treatment of pancreatic NET.   About Surufatinib…


Chi-Med to Discuss Surufatinib Phase III and U.S. Phase I/Ib Efficacy and Safety Data Presented at the 2019 ESMO Annual Meeting

…– – Preparations underway for the potential submission of surufatinib New Drug Application (“NDA”) by year end 2019 for non-pancreatic NET tumors in China – – Treatment options are limited…


Chi-Med Reports 2018 Interim Results and Updates Shareholders on Key Clinical Programs

…Chi‑Med of $32.7 million (H1 2017: net profit $1.7m). Cash resources of $416.9 million at Group level as of June 30, 2018 ($479.6m as of December 31, 2017), including cash…


Chi-Med Highlights Presentations of Surufatinib at the Upcoming AACR Virtual Annual Meetings

…Research (Ministry of Education), Peking University Cancer Hospital & Institute, Beijing, China Session: VPO.CT01 Number: CT142 Link: View Abstract | Download Presentation   Title: Comparison of Pharmacokinetic Profiles and Safety…


Initiation of sulfatinib Phase III registration study in neuroendocrine tumour patients

…placebo-controlled, multi-centre Phase III sulfatinib registration study to treat pathologically low or intermediate grade NET patients whose disease has progressed, locally advanced or distant metastasised and for whom there is…


Chi-Med Announces the NMPA Approval of Surufatinib (Sulanda® in China) for Non-Pancreatic Neuroendocrine Tumors

…trial demonstrated surufatinib reduced risk of progression or death by 67%, extending PFS in all subgroups of non-pancreatic NET patients with an acceptable risk/benefit ratio – – ~400-strong oncology commercial…


Repeat of Announcement of Fifth Public Filing of Registration Statement on Form F-1 and Launch of Potential U.S. Public Offering of ADSs

…price. Chi-Med has applied to have its ADSs approved for listing on the Nasdaq Stock Market under the symbol “HCM.” In addition to the net proceeds which may be generated…


Fifth Public Filing of Registration Statement on Form F-1 and Launch of Potential U.S. Public Offering of ADSs

…Market under the symbol “HCM.” In addition to the net proceeds which may be generated by the Offering, Chi-Med plans to continue to utilize its various resources, including existing cash…


Filing of Registration Statement on Form F-1 for potential Nasdaq Stock Market Listing

…Raise and Offering do proceed, Chi‑Med intends to use the net proceeds of the potential Equity Raise, together with the cash generated by its operations, primarily to advance the clinical…


Final Results for the year ended 31 December 2014

…Results (IFRS11) Revenue up 100% to $91.8 million (2013: $46.0m). Net profit attributable to Chi-Med equity holders of $ 5.4 million (2013: $5.9m) as the Company continues to balance a…


Chi-Med Announces Surufatinib Granted U.S. FDA Fast Track Designations for the Treatment of Both Pancreatic and Non-Pancreatic Neuroendocrine Tumors

…the development of surufatinib, for the treatment of both advanced and progressive pancreatic neuroendocrine tumors (“NET”) and extra-pancreatic (non-pancreatic) NET in patients who are not amenable for surgery. The FDA…


Financial Highlights

…and joint ventures (excluding non-consolidated joint ventures) of Chi-Med. OVERALL GROUP: Group revenue of $204.9 million (2018: $214.1m). Net loss attributable to Chi-Med of $106.0 million (2018: net loss of…


Chi-Med’s New Drug Application for Surufatinib in Non-Pancreatic Neuroendocrine Tumors Granted Priority Review in China

…treatment of non-pancreatic NET. Surufatinib being granted priority review is a positive step forward in potentially bringing this innovative drug to patients, who currently have very limited treatment options.” In…


ESMO2020: Surufatinib for patients with advanced pancreatic NET (SANET-p)

…Department of Gastrointestinal Oncology, The Fifth Medical Center, General Hospital of the PLA Session: Proffered Paper – NETs Abstract Number: 1156O Date & Time: Sunday, September 20, 2020 2:25 PM…


Chi-Med Initiates a Phase IIb/III Trial of Surufatinib in Patients with Unresectable or Metastatic Biliary Tract Cancer in China

…in proof-of-concept clinical trials in the U.S. and several proof-of-concept and late-stage clinical trials in China. Pancreatic NET in China: In 2016, we initiated the SANET-p study, which is a…


Chi-Med Announces Amendment to the 2013 License & Collaboration Agreement on Fruquintinib with Eli Lilly and Company

…as detailed below:   2018 Previous Guidance 2018 Current Guidance Adjustment Group Level: · Consolidated revenue $155-175m $155-175m None · Admin., interest & tax $(16)-(18)m $(16)-(18)m None · Net loss[1]…


Chi-Med Initiates a Phase Ib/II Proof-of-Concept Trial of Sulfatinib in Pancreatic Neuroendocrine Tumors and Biliary Tract Cancer in the United States

…This study follows several trials that are underway in China, including two Phase III studies in pancreatic and non-pancreatic NET that commenced after positive results from a Phase II study,…


Interim Results for the Six Months Ended 30 June 2015

…China Healthcare and Consumer Products Divisions – our Commercial Platform: sales of subsidiaries and JVs up 17%, net profit up 15%. Strong outlook for full year and beyond. London: Tuesday,…


Chi-Med to Discuss Select Global Clinical Trial Data Presented at ASCO20

…tumors (“NET”) Authors: A Dasari, D Li, MW Sung, C Tucci, JS Kauh, MK Kania, AS Paulson Abstract Link: 4610 Preliminary data from the two NET cohorts in the ongoing…


Chi-Med and BeiGene Enter into Clinical Collaboration to Evaluate Combinations of Surufatinib and Fruquintinib with Tislelizumab

…of surufatinib in NET in China, and the ongoing multi-cohort Phase Ib study in the U.S. (clinicaltrials.gov identifier: NCT02549937). In the U.S., surufatinib was granted Fast Track Designations for development…


Chi-Med initiates sulfatinib Phase III registration study in pancreatic neuroendocrine tumor patients

…grade advanced NET whose disease has progressed, locally advanced or distant metastasized and for whom there is no effective therapy. Patients are randomized at a 2:1 ratio to receive either…


ENETS 2017: Sulfatinib Phase Ib/II in Advanced Neuroendocrine Tumors

…sulfatinib monotherapy in patients with advanced grade 1 or 2 advanced NET. 81 patients (41 pancreatic NET and 40 extra-pancreatic NET) were enrolled between November 2014 and January 2016, in…


Chi-Med Announces Surufatinib Granted FDA Orphan Drug Designation for Pancreatic Neuroendocrine Tumors

NET was accepted for review by the China National Medical Products Administration (NMPA) on November 11, 2019.   About FDA Orphan Drug Designation The FDA Orphan Drug Designation Program provides…


Chi-Med Highlights Presentation of Clinical Data from the Successful SANET-ep Phase III Trial at ESMO Annual Meeting

…September 29. Safety and tolerability data presented from an ongoing U.S. Phase Ib study of surufatinib in pancreatic NET patients who have progressed on Sutent® or Afinitor® treatment will also…


Sulfatinib clinical results and fruquintinib-savolitinib combination preclinical results to be presented at the 2015 AACR-NCI-EORTC Molecular Targets and Cancer Therapeutics conference

…objective response rate among the 18 efficacy-evaluable NET patients was 44.4% and disease control rate was 100%. By comparison, sunitinib and everolimus, the two approved single agent therapies for neuroendocrine…


Chi-Med Announces NDA Acceptance in China for Surufatinib in Non-Pancreatic Neuroendocrine Tumors

…the potential approval and launch of surufatinib in China, an important development for NET patients with limited treatment options. In order to maximize patient access to surufatinib upon regulatory approval,…


Chi-Med initiates sulfatinib Phase II clinical trial in thyroid cancer

…and Cancer Therapeutics in early November 2015 (www.chi-med.com/sulfatinib-ph1-eortc-2015/). The Phase I clinical data indicates that sulfatinib has a superior ORR in NET patients. An ORR of 44% was observed for…


Chi-Med Highlights Oral Presentations on Savolitinib Lung Cancer Programs at AACR Annual Meeting

…Resistance Be MET or Will We Not MEK It? Session Type: Clinical Trials Plenary Session Session # & Link: CTPL02 Date & Time: Sunday, March 31: 3:00 PM-5:15 PM Location:…


Dual-listing FAQs

…What does a depositary do? How does it work in practice? How can I buy an ADR or a DI? Can holders of DIs invest in Chi-Med’s ADRs? Can holders…


Chi-Med Presents Further Fruquintinib FRESCO Trial Data at ASCO 2018 Annual Meeting

…Gastrointestinal (Colorectal) Cancer Abstract No. & Link: #3537; abstracts.asco.org/214/AbstView_214_215579.html Poster Link [i]: 16ealJfSDOCUUwuY6Icm22   In FRESCO, fruquintinib demonstrated a statistically significant and clinically meaningful benefit in third-line metastatic CRC patients…


Warning to Shareholders

…or non-existent shares, or offer to buy their shares in a company at an inflated price. The “boiler room” scam has developed over the recent years and there has been…


AACR2020: A Phase I Trial of Surufatinib plus Toripalimab in Patients with Advanced Solid Tumor

…Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Peking University Cancer Hospital & Institute, Beijing, China Session: VPO.CT01 Number: CT142 Link: View Abstract Presenter/Authors Ming Lu, Yanshuo Cao,…


Chi-Med Highlights Clinical Data to be Presented at the Upcoming ESMO Virtual Congress 2020

…of patients with advanced non-pancreatic NET was accepted for review by the China National Medical Products Administration (“NMPA”) and granted Priority Review status in December 2019. A second NDA for…


Chi-Med Highlights Clinical Data to be Presented at the Upcoming ASCO20 Virtual Scientific Program

…be very suitable for possible combinations with other immunotherapies. A New Drug Application (“NDA”) for surufatinib for the treatment of patients with advanced non-pancreatic NET was accepted for review by…


EORTC 2015: First-in-human phase I study of selective VEGFR/FGFR dual inhibitor sulfatinib with milled formulation in patients with advanced solid tumors

…tumours (NETs). Eight NET patients (5 in 300mg QD and 3 in 350mg QD cohort) had confirmed partial response (PR) with median duration of response (DoR) of 13.8 months. The…


Chairman’s Statement

…this year in non-pancreatic NET. Our first NDA for surufatinib was granted Priority Review following our submission in late 2019, and preparation for a second NDA in pancreatic NET is…


Journal of Clinical Oncology: Biomarker-Based Phase II Trial of Savolitinib in Patients With Advanced PRCC

…to savolitinib than a classification based on pathology. These findings justify investigating savolitinib in MET-driven PRCC. Citations and Links Please follow the DOI link to access the publication: J Clin…


Journal of Clinical Oncology: Phase II Trial of Fruquintinib in Patients with Advanced Nonsquamous NSCLC

…an acceptable safety profile. Citations and Links Please follow the DOI link to access the publication: J Clin Oncol.2018 Mar 12:JCO2017767145 DOI link: 10.1200/JCO.2017.76.7145 PubMed unique Identifier link: 29528793…


Fourth Public Filing of Registration Statement on Form F-1 for potential Nasdaq Stock Market Listing

…Article 49(2)(a) to (d) (high net worth companies, unincorporated associations etc) of the Order; or (iv) any other person to whom it may lawfully be communicated (all such persons in…


Third Public Filing of Registration Statement on Form F-1 for potential Nasdaq Stock Market Listing

…(high net worth companies, unincorporated associations etc) of the Order; or (iv) any other person to whom it may lawfully be communicated (all such persons in (i) to (iv) together…


Second Public Filing of Registration Statement on Form F‑1 for potential Nasdaq Stock Market Listing

…(d) (high net worth companies, unincorporated associations etc) of the Order; or (iv) any other person to whom it may lawfully be communicated (all such persons in (i) to (iv)…


Chi-Med Files Application to List in Hong Kong and Announces Proposed Global Offering

…Although the final structure and size of the potential Offering is yet to be determined, Chi-Med expects that the net proceeds from any primary sale of Shares in the Offering,…


Chi-Med Announces Pricing of U.S. Public Offering of ADSs Raising US$262 Million on Nasdaq Global Select Market (RNS)

…October 30, 2017. The net proceeds from the Offering are expected to be used to fund the on-going research and development of the Chi-Med Innovation Platform drug pipeline and for…


Chi-Med Announces that Surufatinib Phase III SANET-p Study Has Already Achieved its Primary Endpoint in Advanced Pancreatic Neuroendocrine Tumors in China and Will Stop Early

…statements reflect Chi-Med’s current expectations regarding future events, including its expectations regarding the NDA approval and launch of surufatinib for the treatment of patients with pancreatic or non-pancreatic NET in…


Phase I clinical data for selective VEGFR, c-Met and VEGFR/FGFR inhibitors to be presented at the 2014 ASCO Annual Meeting

…cohort, 1 liver neuroendocrine tumour (NET) and 1 NET with unknown primary site in 300mg cohort, and 1 lymph node NET in 350mg cohort. ORR is 30% among the 13…


Financial Results

…surufatinib and savolitinib.” Simon To, Chairman, Mar 3, 2020 Read More FY2019 Financial Summary Group US$ Revenue $204.9m Net income/(loss) ($106.0m) — Innovation Platform Revenue $16.0m Net income/(loss) ($133.2m) —…


JAMA: Fruquintinib vs Placebo in Previously Treated Metastatic Colorectal Cancer

…outside of China. Trial Registration ClinicalTrials.gov Identifier: NCT02314819   Citations and Links Please follow the link below to access the publication: JAMA. 2018;319(24):2486-2496. DOI: 10.1001/jama.2018.7855 Link to article: https://jamanetwork.com/journals/jama/article-abstract/2685988…


The Lancet Oncology: Osimertinib plus Savolitinib in EGFRm+, MET+ NSCLC

…on a previous EGFR TKI. This combination might be a potential treatment option for patients with MET-driven resistance to EGFR TKIs.   Citations and Links Please follow the link below…


The Lancet Oncology: Surufatinib SANET-p phase 3 study

…patient population. Funding: Hutchison MediPharma. Trial Registration: ClinicalTrials.gov Identifier: NCT02589821.   Citations and Links Please follow the link below to access the publication: Lancet Oncol. 2020; S1470-2045(20)30493-9. [published online ahead…


Chi-Med Highlights Savolitinib Clinical Data to be Presented at Virtual WCLC

…Han, Center for Lung Cancer, National Cancer Center, Goyang, Republic of Korea Session: FP14 – Targeted Therapy – Clinically Focused Abstract # / Link: #FP14.03 / Link Availability Date: Thursday,…


The Lancet Oncology: Surufatinib SANET-ep phase 3 study

…Funding: Hutchison MediPharma. Trial Registration: ClinicalTrials.gov Identifier: NCT02588170.   Citations and Links Please follow the link below to access the publication: Lancet Oncol. 2020;S1470-2045(20)30496-4. [published online ahead of print, 2020…


Hutchison China MediTech Limited Files Registration Statement for Potential Nasdaq Stock Market Listing

…but has not yet become effective. The ADSs may not be sold, nor may offers to buy be accepted, prior to the time the Registration Statement becomes effective. The Registration…


Hutchison China MediTech Limited Announces Launch of Potential U.S. Public Offering of ADSs

…be sold nor may offers to buy be accepted prior to the time the Form F-1 Registration Statement becomes effective. The Form F-1 Registration Statement and all subsequent amendments may…


Chi-Med Announces Proposed Offering of ADSs (RNS)

…19(5) of the Financial Services and Markets Act 2000 (Financial Promotion) Order 2005, or the Order, (ii) high net worth entities, and other persons to whom it may lawfully be…


Notice of Extraordinary General Meeting and Shareholders’ Circular

…Markets Act 2000 (Financial Promotion) Order 2005 (the “Order”) or (iii) persons falling within Article 49(2)(a) to (d) (high net worth companies, unincorporated associations etc.) of the Order; or (iv)…


Chi-Med Announces the Full Exercise of Underwriters’ Over-allotment Option

…Act 2000 (Financial Promotion) Order 2005, or the Order, (ii) high net worth entities, and other persons to whom it may lawfully be communicated, falling within Article 49(2)(a) to (d)…


Chi-Med Announces the Closing of U.S. Public Offering of American Depositary Shares (ADSs) Raising Approximately US$301.3 Million on the Nasdaq Global Select Market

…Services and Markets Act 2000 (Financial Promotion) Order 2005, or the Order, (ii) high net worth entities, and other persons to whom it may lawfully be communicated, falling within Article…


Chi-Med Announces Pricing of U.S. Public Offering of ADSs Raising US$262 Million on Nasdaq Global Select Market

…The net proceeds from the Offering are expected to be used to fund the on-going research and development of the Chi-Med Innovation Platform drug pipeline and for working capital and…


Chi-Med Announces Pricing of Upsized U.S. Public Secondary Offering of American Depositary Shares

…“Order”) or (iii) are persons falling within Article 49(2)(a) to (d) (high net worth companies, unincorporated associations etc.) of the Order; or (iv) are persons to whom an invitation or…


Closing of U.S. Public Offering of ADSs Raising Approximately US$101 Million on the Nasdaq Stock Market

net worth companies, unincorporated associations etc) of the Order; or (iv) any other person to whom it may lawfully be communicated (all such persons in (i) to (iv) together being…


Final Prospectus

…who fall within Article 49(2)(a) to (d) (high net worth companies, unincorporated associations etc) of the Order; or (iv) any other person to whom it may lawfully be communicated (all…


Pricing of U.S. Public Offering of ADSs

…(d) (high net worth companies, unincorporated associations etc) of the Order; or (iv) any other person to whom it may lawfully be communicated (all such persons in (i) to (iv)…


Chi-Med Presented Pre-clinical Data for Fruquintinib and Sulfatinib at the American Association for Cancer Research Annual Meeting 2017

…underway in China and the United States, including two Phase III studies and one Phase II study in NET patients (SANET-p, SANET-ep and SANET-1), one Phase II study in thyroid…


Chi-Med Initiates a Phase II Study of Sulfatinib in Second-line Biliary Tract Cancer in China

…SANET-p trial is a randomized, double-blind, placebo-controlled, multi-center, Phase III pivotal registration trial to treat about 190 pathologically low or intermediate grade pancreatic NET patients in China whose disease has…


Analyst Coverage

…BofA MERRILL LYNCH Dr. Alec W. Stranahan+1 646 743 2109 alec.stranahan@bofa.com Dr. Geoff Meacham+1 646 855 1004 geoff.meacham@bofa.com BLOOMBERG Cinney Zhangczhang429@bloomberg.net Sam Fazelimfazeli@bloomberg.net CANACCORD GENUITY Dr. John Newman+1…


Chi-Med Announces Pricing of US$110 Million Public Offering of ADSs

…discounts and commissions. The Offering is expected to close on January 27, 2020, subject to customary closing conditions. Chi-Med will receive all of the net proceeds from the sale of…


Bloomberg

…Cinney Zhang czhang429@bloomberg.net Sam Fazeli mfazeli@bloomberg.net


Chi-Med Announces Proposed Public Offering of ADSs

…for the Offering has not yet been determined. Chi-Med will receive all of the net proceeds from the sale of ADSs in the Offering, if completed, which it intends to…


Clinical Project Manager

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Deutsche Bank ADR Virtual Investor Conference (dbVIC)

…Live virtual investor conference. An on-demand archive is available for 90 days. TIME: 9am Eastern Standard Time LINK: www.adr.db.com/dbvic…


ASCO 2018: Colorectal cancer Q-TWiST with fruquintinib treatment in FRESCO

…Session: Gastrointestinal (Colorectal) Cancer Abstract No. & Link: #3544; abstracts.asco.org/214/AbstView_214_224293.html Copies of this poster can be obtained from American Society of Clinical Oncology and the author of the poster….


The Royal Society of Medicine 15th Medical Innovations Summit

…The Royal Society of Medicine, London, UK Please visit rsm.ac.uk for more information. A video recording of the 20-minute presentation is available. RSM video link Note: there is…


Tax Strategy

…which is listed on The Stock Exchange of Hong Kong. The CKHH tax strategy for the CKHH Group can be found on the website of CKHH via the link here….


Deutsche Bank ADR Virtual Investor Conference (dbVIC)

…  Live virtual investor conference. TIME: 9:30am Eastern Daylight Time LINK: www.adr.db.com/dbvic…


ASCO 2018: Subgroup analysis by prior anti-VEGF or anti-EGFR target therapy in FRESCO

…Hall A, Poster Board: #30 Session: Gastrointestinal (Colorectal) Cancer Abstract No. & Link: #3537; abstracts.asco.org/214/AbstView_214_215579.html Copies of this poster may be obtained from the American Society of Clinical Oncology….


AACR2020: Comparison of Pharmacokinetic Profiles and Safety of Surufatinib in Patients from China and the United States

…Center, Duarte, CA, USA. Session: VPO.CT01 Number: CT115 Link: View Abstract Presenter/Authors John Kauh. Hutchison MediPharma International Inc, Florham Park, NJ   Disclosures J. Kauh: ; Hutchison MediPharma International Inc….


Hong Kong Listing

Press Release Group | 15 Apr 2019 Chi-Med Files Application to List in Hong Kong and Announces Proposed Global Offering Listing Documents Redacted form of the draft…


Remuneration Committee – Terms of Reference

…other limits or discretions should be identified and explained at the time of approving the policy; 10.3.5. proportionality – the link between individual awards, the delivery of strategy and the…


Chi-Med Highlights HMPL-689 Clinical Data to be Presented at the 62nd ASH Annual Meeting

…# / Link: #1135 / https://doi.org/10.1182/blood-2020-136013 Date & Time: Saturday, December 5, 2020, 7:00 AM – 3:30 PM (PT)   About HMPL-689 HMPL-689 is a novel, selective oral inhibitor targeting…


ASH2020: Results from a Phase 1 Dose Escalation Study of HMPL-689, a Selective Oral PI3Kδ Inhibitor, in Chinese Patients with Relapsed/Refractory Lymphomas

…Cell, Follicular, and Other Indolent B-Cell Lymphoma – Clinical Studies: Poster I Abstract # / Link: #1135 / https://doi.org/10.1182/blood-2020-136013 Date & Time: Saturday, December 5, 2020, 7:00 AM – 3:30…


Disclaimer

…of the holder’s rights. Hutchison China MediTech Limited and its affiliated companies assume no responsibility for material created or published by third parties that are referenced by a link from…


dbVIC – Deutsche Bank American Depositary Receipt (ADR) Virtual Investor Conference

…Live virtual investor conference. An on-demand archive is available for 90 days. TIME: 9.00am Eastern Standard Time LINK: www.adr.db.com/dbvic…