1月11日，由中国医药教育协会主办、北京同仁医院承办的2026"近视防控追光计划科普教育行动"公益 活动在北京同仁医院亦庄院区成功举办。本次活动以"1路相伴、2重守护、4季无忧"为主题，聚焦儿童 青少年近视防控这一社会热点问题，通过科普讲座、互动问答、健康咨询等丰富形式，为广大亲子家庭 传递科学实用的护眼知识。 来源：环球网 当前，儿童青少年近视已成为全社会共同关注的问题。据世界卫生组织新研究报告显示，我国近视总人 数约6 亿，其中儿童青少年近视人数占比高达50%-60%，近视低龄化、重度化问题突出，亟需全社会凝 聚共识、协同发力。2025年12月底，国家卫健委等十三部门联合发布《儿童青少年"五健"促进行动计划 （2026—2030年）》提出，"实施分级分类干预"儿童青少年视力健康促进行动2030年目标，进一步聚焦 通过科学评估和差异化管理，有效降低儿童青少年近视发生率，并设定了一系列具体目标。 在此背景下，本次活动邀请北京同仁医院、北京朝阳医院、北京儿童医院等多家首都医院知名眼科专家 学者围绕科学防控知识传播、进一步提升公众对近视防控的认知水平；同时以创新形式强化社会关注， 激发家庭、学校、医疗机构等多方主 ...

（来源：经济参考报） 因具有延缓儿童近视进展的作用，低浓度阿托品滴眼液被不少家长熟知。近日，两款"浓度翻倍版本"的 低浓度硫酸阿托品滴眼液获批上市，引发家长们对这一药品的关注——孩子近视了都可以用"阿托 品"吗？它是近视"后悔药"吗？对此，记者采访了相关专家。 广西医科大学第一附属医院眼科副主任医师黎霞介绍，阿托品是一种睫状肌麻痹剂，以往常在验光检查 中作为散瞳药使用。近年研究发现，低浓度阿托品滴眼液具有延缓近视进展的作用，其机制可能与抑制 眼轴增长、调节视网膜信号传导有关，"相关药品受到关注，反映出公众对近视防控的迫切需求"。 这两款新获批硫酸阿托品滴眼液浓度分别为0.02%和0.04%，此前我国首款获批用于延缓儿童近视进展 的低浓度阿托品于2024年上市。中国工程院院士、北京同仁眼科中心主任王宁利是本次获批产品临床试 验主要研究者。"从'单一浓度'变成了'浓度量身定制'，让'个性化防控'成为现实，儿童的近视防控干预 效果将进一步提升。"他说。 效果与安全是家长最关注的问题。北京同仁医院斜视与小儿眼科主任医师付晶介绍，从防控效果来看， 临床研究显示，在规范使用和密切随访的前提下，相较于0.01%阿托品滴眼液 ...

日前，兴齐眼药（300573.SZ）公告称，0.02%（0.4ml：0.08mg）及0.04%（0.4ml：0.16mg）硫酸阿托 品滴眼液的补充申请获得国家药品监督管理局批准，用于延缓球镜度数为-1.00D至-4.00D(散光≤1.50D、 屈光参差≤1.50D)的6至12岁儿童的近视进展。 当前我国儿童青少年近视问题形势严峻，不仅呈现"低龄、高发、重度"的发展态势，中度、高度近视增 长趋势亦持续显现。兴齐眼药方面指出，此次两款阶梯浓度产品的获批，成为兴齐眼药继2024年0.01% 浓度硫酸阿托品滴眼液获批后的重要突破，进一步丰富了临床治疗选择。 利好消息迅速传导至资本市场。1月5日，兴齐眼药股价收涨4.82%，报73.68元/股；1月6日股价延续上 行态势，报74.2元/股收盘，上涨0.71%，总市值达182.85亿元；1月7日，兴齐眼药股价再度上涨0.84%。 在业内看来，目前国内外尚无0.02%和0.04%硫酸阿托品滴眼液近视相关适应症产品获批上市，且兴齐 眼药0.01%硫酸阿托品滴眼液（美欧品^®）作为国内首款获批用于延缓儿童近视进展的产品，已积累了 稳定的市场份额和临床认可度，这将为两款新品打开市 ...

记者丨 韩利明 编辑丨季媛媛 1月4日晚间，兴齐眼药（300573.SZ）公告称，0.02%（0.4ml：0.08mg）及0.04%（0.4ml： 0.16mg）硫酸阿托品滴眼液的补充申请获得国家药品监督管理局批准，用于延缓球镜度数 为-1.00D至-4.00D(散光≤1.50D、屈光参差≤1.50D)的6至12岁儿童的近视进展。 当前我国儿童青少年近视问题形势严峻，不仅呈现"低龄、高发、重度"的发展态势，中度、高 度近视增长趋势亦持续显现。兴齐眼药方面指出，此次两款阶梯浓度产品的获批，成为兴齐眼 利好消息迅速传导至资本市场。1月5日兴齐眼药股价直线冲高，最终收涨近5%，报73.68元/ 股；1月6日股价延续上行态势，报74.2元/股收盘，上涨0.71%，总市值达182.85亿元。 药继2024年0.01%浓度硫酸阿托品滴眼液获批后的重要突破，进一步丰富了临床治疗选择。 在业内看来，目前国内外尚无0.02%和0.04%硫酸阿托品滴眼液近视相关适应症产品获批上 市，且兴齐眼药0.01%硫酸阿托品滴眼液（美欧品®）作为国内首款获批用于延缓儿童近视进 展的产品，已积累了稳定的市场份额和临床认可度，这将为两款新品打开 ...

21世纪经济报道记者韩利明 1月4日晚间，兴齐眼药（300573.SZ）公告称，0.02%（0.4ml：0.08mg）及0.04%（0.4ml：0.16mg）硫 酸阿托品滴眼液的补充申请获得国家药品监督管理局批准，用于延缓球镜度数为-1.00D至-4.00D(散光 ≤1.50D、屈光参差≤1.50D)的6至12岁儿童的近视进展。 当前我国儿童青少年近视问题形势严峻，不仅呈现"低龄、高发、重度"的发展态势，中度、高度近视增 长趋势亦持续显现。兴齐眼药方面指出，此次两款阶梯浓度产品的获批，成为兴齐眼药继2024年0.01% 浓度硫酸阿托品滴眼液获批后的重要突破，进一步丰富了临床治疗选择。 图片来源：兴齐眼药公告 利好消息迅速传导至资本市场。1月5日，兴齐眼药股价收涨4.82%，报73.68元/股；1月6日股价延续上 行态势，报74.2元/股收盘，上涨0.71%，总市值达182.85亿元。 在业内看来，目前国内外尚无0.02%和0.04%硫酸阿托品滴眼液近视相关适应症产品获批上市，且兴齐 眼药0.01%硫酸阿托品滴眼液（美欧品®）作为国内首款获批用于延缓儿童近视进展的产品，已积累了 稳定的市场份额和临床认可度，这将 ...

作为一款需长期使用的药物，其安全性与有效性是家长最为关心的核心。"0.02%与0.04%硫酸阿托品滴 眼液，是建立在0.01%浓度基础上长期系统性研究的深化成果。"兴齐眼药副总经理、研发负责人杨强 介绍，在获得药物临床试验批准后，企业开展了一项关于0.02%和0.04%阿托品滴眼液的III期临床研 究，研究采用多中心、随机、双盲、安慰剂平行对照、优效性设计的试验方法，共28家中心随机入组 800例，给药期2年，停药观察期1年。研究结果显示，0.02%和0.04%阿托品滴眼液与安慰剂相比，均能 够有效延缓儿童近视进展，且总体安全性良好。 作为国内专注于眼科药物研发、具备全产业链优势的创新型制造企业，兴齐眼药长期关注未被满足的临 床需求，是国内最早开展阿托品滴眼液用于延缓近视进展临床研究的企业：早在2014年即立项开发低浓 度硫酸阿托品，并于2016年与新加坡全国眼科中心达成合作，引入ATOM2临床数据，系统开展从药 理、药代到Ⅲ期临床的完整研究。在此过程中，兴齐眼药逐步积累了关于不同浓度阿托品在近视防控中 的疗效与安全性数据，并采用独家MYOSTAFORT稳适创新技术，实现制剂稳定、点眼舒适且不含抑菌 剂，为多 ...

Core Insights - The company, Yuan Da Pharmaceutical Group, has made significant progress in the field of myopia prevention for children with its innovative ophthalmic drug GPN00884, which has entered the important phase of exploring dosage and assessing preliminary efficacy after completing patient enrollment in a Phase IIa clinical study in China [1][2] Group 1: Clinical Development - GPN00884 has completed patient enrollment for its Phase I clinical study in China by August 2024 and is expected to complete the study by March 2025 [2] - The ongoing Phase IIa clinical trial is a randomized, double-blind, placebo-controlled study aiming to enroll over 80 myopic participants aged 6 to 12 years to evaluate the drug's effectiveness and safety [2] Group 2: Market Potential - The global market for myopia treatment drugs is projected to reach nearly $5 billion by 2033, with the Chinese market accounting for approximately $1.7 billion [1] - There is a significant unmet clinical need for effective myopia treatments, as current options like low-concentration atropine eye drops have high incidences of side effects, affecting patient compliance [1] Group 3: Strategic Focus - Yuan Da Pharmaceutical is focusing on ophthalmology as a key strategic development area, continuously innovating in ophthalmic drugs to enhance its industry position and market competitiveness [2] - The company has established a comprehensive product system for innovative drugs, combining partnerships and in-house research to develop treatments for various eye conditions, including dry eye syndrome and myopia [2][3] Group 4: Recent Achievements - The company has recently achieved significant clinical advancements with three products this year, including an innovative nasal spray for dry eye syndrome and treatments for other eye conditions [3] - Multiple innovative products are expected to be approved for market launch in the next three years [3]

Core Viewpoint - The recent progress of Yuan Da Pharmaceutical in the field of myopia prevention and control is significant, with the initiation of the IIa clinical trial for the innovative ophthalmic drug GPN00884, which aims to delay the progression of myopia in children [1][3]. Group 1: Market Context - Myopia is a major public health issue globally, with 2.6 billion people affected as of 2020, including 312 million under the age of 19 [2]. - China has the highest number of myopia cases in the world, with a reported prevalence rate of 51.9% among children and adolescents in 2022 [2]. - The Chinese government has prioritized myopia prevention as a national strategy, implementing various plans and guidelines to combat the issue [2]. Group 2: Product Development - GPN00884 is positioned as a potential breakthrough in myopia treatment, as it does not cause adverse effects such as photophobia or pupil dilation, which are common with existing treatments like low-concentration atropine eye drops [3]. - The IIa clinical trial for GPN00884 will involve over 80 participants aged 6 to 12, focusing on evaluating its efficacy and safety in delaying myopia progression [3]. - Previous phases of clinical trials for GPN00884 have shown good safety and tolerability profiles, indicating its potential for successful market entry [3]. Group 3: Competitive Advantage - The successful initiation of the IIa clinical trial enhances Yuan Da Pharmaceutical's competitive edge in the myopia prevention market, addressing the urgent need for safe and effective treatment options for children [4]. - The company has established a comprehensive product pipeline in the ophthalmic sector, focusing on innovative drug development to strengthen its market position [5]. - Yuan Da Pharmaceutical's strategy includes a combination of in-house development and partnerships to create a diverse range of ophthalmic products, enhancing its competitive differentiation [5]. Group 4: Future Prospects - The company anticipates significant growth in its ophthalmic product pipeline, with multiple innovative products expected to receive regulatory approval in the coming years [8]. - Recent advancements include the launch of OC-01 for dry eye treatment and TP-03 for demodex blepharitis, both of which are expected to contribute to the company's revenue growth [8][9]. - The ongoing development of these products not only showcases Yuan Da Pharmaceutical's competitive capabilities but also aligns with its "Go Global" strategy, potentially expanding its market reach internationally [9].

Core Viewpoint - Xingqi Eye Pharmaceutical (300573.SZ) reported impressive financial results for 2024 and Q1 2025, particularly with the low-concentration atropine product, which has become a key revenue driver, accounting for over 10% of total revenue. However, the performance of atropine in 2024 fell short of broker expectations, raising questions about the sustainability of the company's leading position as competitors enter the market [1][2][11]. Financial Performance - In 2024, the company achieved a revenue of 1.943 billion yuan, representing a year-on-year growth of 32.42%, with a net profit of 338 million yuan, up 40.84% year-on-year. For Q1 2025, revenue reached 536 million yuan, a significant increase of 53.24%, and net profit soared by 319.86% to 146 million yuan [1][2][11]. - The company's distribution plan for 2024 includes a 10-for-4 stock split and a cash dividend of 10 yuan [1]. Product Overview - Xingqi Eye Pharmaceutical specializes in ophthalmic drugs, with a portfolio of 60 approved ophthalmic products, 38 of which are included in the medical insurance directory, and 6 in the national essential drug list [2][3]. - The company's eye drops segment saw a revenue increase of 106.08% in 2024, with key products including Cyclosporine Eye Drops and Sulfate Atropine Eye Drops, both contributing significantly to revenue [6][11]. Market Dynamics - The demand for eye drops is evident, particularly among children and adolescents, with a near 52% myopia rate reported among Chinese youth [6]. The low-concentration atropine eye drops, approved in March 2024, are expected to reshape the ophthalmic drug market, with a projected peak sales of 10.18 billion yuan by 2027 [10][11]. - The company has established a comprehensive sales network, collaborating with numerous private and public healthcare institutions, and is actively expanding its presence in e-commerce and internet healthcare [12][13]. Competitive Landscape - The uniqueness of Xingqi's atropine product is threatened as other companies, including Heng Rui Pharmaceutical and Zhaoke Ophthalmology, are entering the market with similar products [14][22]. Heng Rui's product is expected to be launched by 2027, indicating increasing competition [18]. - The competitive landscape is evolving, with multiple companies pursuing the development of atropine eye drops, which may impact Xingqi's market share and pricing power in the future [23].