Delving into the Latest Updates on Jaktinib Hydrochloride with Synapse

Overview

Basic Info

Drug Type

Small molecule drug

Synonyms

Gecacitinib Hydrochloride, Jakotinib hydrochloride, Jaktinib

+ [3]

Target

ALK2 x JAK1 x JAK2 x JAK3 x TYK2

Mechanism

ALK2 inhibitors(Activin receptor type-1 inhibitors), JAK1 inhibitors(Tyrosine-protein kinase JAK1 inhibitors), JAK2 inhibitors(Tyrosine-protein kinase JAK2 inhibitors)

+ [2]

Therapeutic Areas

Hemic and Lymphatic DiseasesOther DiseasesImmune System Diseases+ [4]

Active Indication

Post-essential thrombocythemia myelofibrosisPost-polycythemia vera myelofibrosisPrimary Myelofibrosis+ [11]

Inactive Indication

Bone Marrow NeoplasmsInflammatory Bowel DiseasesMycosis Fungoides+ [2]

Originator Organization

Suzhou Zelgen Biopharmaceuticals Co., Ltd.

Active Organization

Suzhou Zelgen Biopharmaceuticals Co., Ltd.

Inactive Organization-

Drug Highest PhaseNDA/BLA

First Approval Date-

RegulationSpecial Review Project (CN), Orphan Drug (US)

Structure

Molecular FormulaC23H25ClN6O3

InChIKeyPXDNVDFBKNFZEE-URSAUJDJSA-N

CAS Registry2056097-81-3

Author: Suo, Shanshan ; Zhu, Huanling ; Wu, Dengshu ; Zhou, Hu ; Jin, Jie ; Xia, Ruixiang ; Hu, Yu ; Jiang, Zhongxing ; Yu, Wenjuan ; Yin, Hewen ; Wang, Xiuli ; Jin, Chenghao ; Li, Wei ; Wu, Liqing ; Zhou, Zeping ; Liu, Jing ; Zhang, Feng ; Sun, Kai ; Zhuang, Junling ; Zhang, Yi ; Yang, Linhua ; Li, Fei ; Huang, Jinwen ; Hu, Jianda ; Jiang, Qian ; Li, Yan ; Du, Xin

Jaktinib, a novel JAK and ACVR1 inhibitor, has exhibited promising results in treating patients with myelofibrosis (MF). ZGJAK002 is a Phase 2 trial aimed to assess the efficacy and safety of jaktinib 100 mg BID (N = 66) and 200 mg QD (N = 52) in JAK inhibitor-naive patients with intermediate- or high-risk MF. We herein present the long-term data with a median follow-up of 30.7 months. At data cutoff, 30.3% of patients in 100 mg BID and 28.8% in 200 mg QD were still continuing their treatment. The 100 mg BID group displayed a numerically higher best spleen response compared with the 200 mg QD group (69.7% vs. 46.2%), with 50.4% from the BID and 51.2% from the QD group maintaining spleen responses over 120 weeks. The 36-month survival rates were 78.2% in BID and 73.6% in QD group. The tolerability of jaktinib remained well, and common grade ≥3 adverse drug reactions included anemia (15.2% vs. 21.2%), thrombocytopenia (15.2% vs. 11.5%), and infectious pneumonia (10.6% vs. 1.9%) in BID and QD groups, respectively. By comparing the two groups, the incidence of adverse events (AEs) were similar, except for drug-related serious AEs (24.2% vs. 9.6%) and AEs leading to treatment discontinuation (15.2% vs. 7.7%), which were higher in BID group. The percentages of AEs resulting in death were comparable, with 6.1% in BID and 5.8% in QD group. These analyses further support the long-term durable efficacy and acceptable safety of jaktinib at 100 mg BID and 200 mg QD doses for treating MF.

02 Jan 2024·Expert Opinion on Investigational Drugs

Treatment of anemia in myelofibrosis: focusing on novel therapeutic options

Review

Author: Arslan Davulcu, Eren ; Eşkazan, Ahmet Emre ; Kılıç, Emre ; Oğuz, Merve Beyza

INTRODUCTIONMyelofibrosis is a clonal myeloproliferative neoplasm associated with the proliferation of hematopoietic stem cells, increased bone marrow fibrosis, extramedullary hematopoiesis, hepatosplenomegaly, abnormal cytokine production, and constitutional symptoms. These and many other factors contribute to the development of anemia in myelofibrosis patients.AREAS COVEREDThis review summarizes novel and promising treatments for anemia in myelofibrosis including transforming growth factor-β inhibitors luspatercept and KER-050, JAK inhibitors momelotinib, pacritinib, and jaktinib, BET inhibitors pelabresib and ABBV-744, antifibrotic PRM-151, BCL2/BCL-XL inhibitor navitoclax, and telomerase inhibitor imetelstat.EXPERT OPINIONStandard approaches to treat myelofibrosis-related anemia have limited efficacy and are associated with toxicity. New drugs have shown positive results in myelofibrosis-associated anemia when used alone or in combination.

03 Oct 2023·Expert Opinion on Investigational Drugs

Novel Janus-kinase (JAK) Inhibitors in Myelofibrosis

Review

Author: Eskazan, Ahmet Emre ; Ipek, Yildiz ; Kilic, Berkay ; Gunay, Ulgar Boran

INTRODUCTIONJAK inhibitors (JAKis), used in the treatment of myelofibrosis, have entered standard treatment, providing significant improvements in spleen size and symptom burden. Although splenomegaly provides a reduction and some improvement in cytopenia, there is still a way to go. Novel JAKis are being investigated to overcome barriers to treatment access, such as therapeutic challenges, intolerance, and unresponsiveness.AREAS COVEREDThis review includes the current status of JAKi treatment for myelofibrosis, mainly focusing on investigational JAKis; jaktinib, lestaurtinib, itacitinib, gandotinib, BMS-911543, ilginatinib, TQ05105, and flonoltinib maleate. MEDLINE and clinicaltrials.gov were screened to identify all completed or active studies on this topic. The outcomes of the preclinical studies and clinical trials are presented and discussed for each drug.EXPERT OPINIONIn patients with myelofibrosis, momelotinib was effective in treating anemia, whereas jaktinib was effective in both anemia and Total Symptom Score (TSS). More phase 3 studies are needed to provide more precise evidence. The increasing variety of JAKis will allow for more personalized treatment options for myelofibrosis in the future. The potential impact on disease progression, molecular responses, and the duration of this response will become important parameters for future evaluations of these drugs.

1

News (Medical) associated with Jaktinib Hydrochloride

18 Jun 2021

·www.globenewswire.com

Axial Spondyloarthritis Pipeline: Drug Pipeline, Regulatory Events and Clinical Trials in the Spotlight| Insights by DelveInsight

Los Angeles, June 17, 2021 (GLOBE NEWSWIRE) -- Axial Spondyloarthritis Pipeline: Drug Pipeline, Regulatory Events and Clinical Trials in the Spotlight| Insights by DelveInsight The report offers the most up-to-date information on Axial Spondyloarthritis pipeline products being developed by notable companies such as Pfizer, Suzhou Zelgen Biopharmaceuticals, Clover Biopharmaceuticals, FunPep Co Ltd., Kinevant Sciences, Izana Bioscience, Mycenax Biotech, and UCB Biopharma, among others. DelveInsight’s ‘Axial Spondyloarthritis (axSpA) Pipeline Insights’ report offers exhaustive coverage of the emerging therapies in different stages of development from pre-clinical till late-stage, along with dormant, inactive, and abandoned therapeutic agents. Some of the important takeaways from the Axial Spondyloarthritis Pipeline report: Request for Sample to know more about the therapies expected to make grab the maximum patient pool @ Axial Spondyloarthritis Emerging Therapies and Forecast The Axial Spondyloarthritis Pipeline reports lay down a thorough coverage of the ongoing clinical trials, collaborations taking place in the domain, recent happenings in the Axial Spondyloarthritis pipeline space, and growth prospects across the Axial Spondyloarthritis domain. Axial Spondyloarthritis: Overview Axial Spondyloarthritis is a chronic, inflammatory rheumatic disease that affects primarily the axial joints leading to severe pain, stiffness, and fatigue. It starts with an early inflammatory phase in which there is no structural damage in the sacroiliac joints (non-radiographic disease) progressing to later stages in which structural damage is visible on X‑ray scans of the sacroiliac joints as erosions, sclerosis, or bony bridges (radiographic disease; also known as Ankylosing Spondylitis). Discover more about the disease, treatments, and pipeline therapies @ axSpA Pipeline Assessment Axial Spondyloarthritis Pipeline Drugs Request for Sample to know more @ Axial Spondyloarthritis Pipeline Analysis, Key Companies, and Futuristic Trends Axial Spondyloarthritis Therapeutics Assessment The Axial Spondyloarthritis Pipeline report presents a kaleidoscopic view of the axSpA emerging novel therapies segmented by Stage, Product Type, Route of Administration (RoA), Molecule Type, Target, and Mechanism of Action. By Product Type By Stage By Molecule Type By Route of Administration By Mechanism of Action By Targets For rich insights into merging therapies and assessment, visit Axial Spondyloarthritis Pipeline: Emerging Novel Therapies Scope of the Axial Spondyloarthritis Pipeline Report Coverage: GlobalKey Players: Izana Bioscience, UCB, Sun Pharma Global, Akeso Biopharma, Kinevant Sciences, Jiangsu Hengrui Medicine Co., Suzhou Zelgen Biopharmaceuticals, Clover Biopharmaceuticals, Mycenax Biotech, Boehringer Ingelheim, and Qyuns Therapeutics among others.Key Axial Spondyloarthritis Pipeline Therapies: Namilumab , Bimekizumab, Tofacitinib, Tildrakizumab, AK-111, NDI 031232, Gimsilumab, QX002N, SHR-0302, Jaktinib, SCB-808, FPP003, KIN-1901, ENIA11, BI 730357, and QX002N among others. Discover more about the report offerings @ axSpA Emerging Therapies, Treatments, and Ongoing Clinical Trials Table of Contents Get in touch with our Business executive for Regulatory Analysis, Licensing Services, and Consulting Solutions Related Reports Axial Spondyloarthritis MarketDelveInsight's "Axial Spondyloarthritis Market Insights, Epidemiology, and Market Forecast-2030" report. Non-Radiographic Axial Spondyloarthritis MarketDelveInsight's "Non-Radiographic Axial Spondyloarthritis (nr-AxSpA) Market Insights, Epidemiology, and Market Forecast-2030" report. Spondylolisthesis Market InsightsDelveInsight's “Spondylolisthesis Market Insights, Epidemiology, and Market Forecast-2030" report. Ankylosing Spondylitis MarketDelveInsight’s ‘Ankylosing Spondylitis Market Insights, Epidemiology, and Market Forecast–2030’ report. Global Kinase Inhibitor In Autoimmune Diseases MarketDelveInsight’s ‘Global Kinase Inhibitor in Autoimmune Diseases Market Insights and Market Forecast – 2030’ report. Adenosine Deaminase Severe Combined Immunodeficiency MarketDelveInsight's "Adenosine Deaminase-Severe Combined Immunodeficiency Market Insights, Epidemiology, and Market Forecast-2030" report. Adult-Onset Still Disease MarketDelveInsight’s “Adult-onset Still’s Disease Market Insights, Epidemiology, and Market Forecast – 2030” report. Browse through our posts ABSSSI Pipeline Analysis Parkinson's Disease Risk FactorsWearable Healthcare Devices Market About DelveInsight DelveInsight is a leading Business Consultant and Market Research firm focused exclusively on life sciences. It supports Pharma companies by providing comprehensive end-to-end solutions to improve their performance. Get hassle-free access to all the healthcare and pharma market research reports through our subscription-based platform PharmDelve. For more insights, visit Pharma, Healthcare, and Biotech News

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R&D Status

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Indication	Highest Phase	Country/Location	Organization	Date
Post-essential thrombocythemia myelofibrosis	NDA/BLA	CN	Suzhou Zelgen Biopharmaceuticals Co., Ltd.	17 Oct 2022
Post-polycythemia vera myelofibrosis	NDA/BLA	CN	Suzhou Zelgen Biopharmaceuticals Co., Ltd.	17 Oct 2022
Primary Myelofibrosis	NDA/BLA	CN	Suzhou Zelgen Biopharmaceuticals Co., Ltd.	17 Oct 2022
Ankylosing Spondylitis	Phase 3	CN	Suzhou Zelgen Biopharmaceuticals Co., Ltd.	19 Jun 2023
Acute Graft Versus Host Disease	Phase 3	CN	Suzhou Zelgen Biopharmaceuticals Co., Ltd.	14 Jul 2022
Dermatitis, Atopic	Phase 3	CN	Suzhou Zelgen Biopharmaceuticals Co., Ltd.	07 Jul 2022
Alopecia Areata	Phase 3	CN	Suzhou Zelgen Biopharmaceuticals Co., Ltd.	01 Sep 2021
Myelofibrosis	Phase 3	CN	Suzhou Zelgen Biopharmaceuticals Co., Ltd.	22 Jan 2021
Plaque psoriasis	Phase 2	CN	Suzhou Zelgen Biopharmaceuticals Co., Ltd.	02 Mar 2021
Idiopathic Pulmonary Fibrosis	Phase 2	CN	Suzhou Zelgen Biopharmaceuticals Co., Ltd.	13 Aug 2020

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Clinical Result

Indication

Phase

Evaluation

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Study	Phase	Population	Analyzed Enrollment	Group	Results	Evaluation	Publication Date


NCT05051761 (ZGJAK018, NEWS) Manual	Phase 3	Alopecia Areata	425	吉卡昔替尼 50mg	(mczoejnxpc) = 吉卡昔替尼治疗重症斑秃患者的安全性与耐受性良好 pbmsdrrwmz (brvqrquvjc )	Positive	13 Jun 2024
				吉卡昔替尼 75mg
NCT04217993 (ZGJAK006, ASCO2024)	Phase 2	Myelofibrosis ferritin \| hemoglobin	39	jaktinib	(smdgivffqf) = fqixbfkycg zpigsobvcb (ktccstgrzn ) View more	Positive	24 May 2024
				jaktinib	(smdgivffqf) = gejyinilbq zpigsobvcb (ktccstgrzn ) View more
NCT04617028 (ZGJAK016, EHA2024)	Phase 3	Primary Myelofibrosis First line	105	Jaktinib 100 mg bid	(rcpyfydggi) = wtjgxvpafa rcfmuljuje (bfbmfqzrbg ) View more	Positive	14 May 2024
				Hydroxyurea (HU) 500 mg bid	(rcpyfydggi) = okmgoejidm rcfmuljuje (bfbmfqzrbg ) View more
ZGJAK002, ZGJAK006, ZGJAK017 (EHA2024)	Phase 2	JAK2 V617F mutation	118	Jaktinib 100 mg bid	kdwaatolwg(rxvtbvvdkg) = gcawvsgrnm fwjgoaqhus (wzzfkgugns ) View more	Positive	14 May 2024
ZGJAK002 (ASH2023)	Phase 2	Mycosis Fungoides	118	Jaktinib 100 mg BID	(qlewizyvbq) = xvmapopbfx pimpmwdovs (qoglquoxwg, 55.9% - 81.2%)	Positive	09 Dec 2023
				Jaktinib 200 mg QD	(qlewizyvbq) = escshswupj pimpmwdovs (qoglquoxwg, 40.9% - 73.0%)
NCT04539639 (EADV2023)	Phase 2	Dermatitis, Atopic	166	Jaktinib 50mg Bid	yupopblead(yyzvbqnywo) = hrnblvhiue pecoqcjphs (lwewcgalha ) View more	Positive	11 Oct 2023
				Jaktinib 75mg Bid	yupopblead(yyzvbqnywo) = wukuykofie pecoqcjphs (lwewcgalha ) View more
NCT04851535 (ZGJAK017, NEWS) Manual	Phase 2	Myelofibrosis	34	盐酸杰克替尼 100 mg Bid	(ftxicheyhd) = krejoobqkk qaripzacpe (dhazodutah ) View more	Positive	12 Jul 2023
EHA2023	Phase 2	Myelofibrosis	44	Jaktinib 100 mg	(nlvyrdndsj) = hfjyhnmnxh pttfhfspbf (mahjlztqgk ) View more	-	08 Jun 2023
EHA2023	Phase 3	Primary Myelofibrosis	253	Jaktinib 100 mg	(alhmvqcjxf) = gswywwdcdx pxsilymxsa (kwscmszeev ) View more	-	08 Jun 2023
				Hydroxyurea 0.5 g	(alhmvqcjxf) = gndxsdlmeq pxsilymxsa (kwscmszeev ) View more
EHA2023	Phase 2	Myelofibrosis	34	Jaktinib 100 mg bid	(amuaycujce) = ztcbroqulk pcymcuvmex (anxuiyilqj ) View more	-	08 Jun 2023