Enzeshu® (Suvisexumab for Injection) is co-developed by Simcere Zaiming and Pyxis Oncology. Simcere Zaiming completed its preclinical and clinical studies, executed cell line screening and process development using proprietary technology platforms, and manufactured clinical trial supplies. Post-approval, commercial production will be conducted at Simcere Zaiming’s antibody facility in Nanjing Jiangbei New Area.

As a recombinant humanized anti-VEGF monoclonal antibody, Enzeshu® exerts antitumor effects by precisely blocking VEGF-receptor binding to inhibit tumor angiogenesis. It is China’s first anti-angiogenic targeted drug approved for the full platinum-resistant ovarian cancer population, transcending the historically limited therapeutic landscape in this field.

Cosela® (trilaciclib hydrochloride for injection) is the world's first innovative drug jointly developed by Simcere and G1 Therapeutics, which is administered before chemotherapy for comprehensive myeloprotection against chemotherapy damages and was certified as a "Breakthrough Therapy" by FDA. It was launched in the United States in Feb. 2021. In Aug. 2020, Simcere entered into an exclusive license agreement with G1 to obtain rights for the development and commercialization of Cosela® for all indications in Greater China.

A pivotal phase Ⅱ clinical study, led by Professor Lin Shen from Peking University Cancer Hospital and Institute，has evaluated the efficacy and safety of Envafolimab in patients with advanced dMMR/MSI-H tumors. The updated clinical data presented at CSCO 2021 showed that the Objective Response Rate (ORR) of patients who received Envafolimab as second or later-line treatment is 44.7%, including 12 (11.7%) cases of Complete Response (CR). The responses were durable, and the rates of durable response at 12 months in patients with advanced colorectal cancer (CRC), advanced gastric cancer, other advanced solid tumors, and all patients were 89.3%, 100%, 100%, and 93.2%, respectively. The median progression-free survival (PFS) was 11.1 months, 12-month overall survival (OS) rate was 73.6%. Envafolimab was well tolerated in this study with no cases of immune-related pneumonitis, immune-related colitis, immune-related nephritis, or infusion related reactions reported.

At present, Envafolimab is being studied in clinical trials in multiple tumor types in China, the United States and Japan, including registration/phaseⅢclinical trials in multiple indications. Envafolimab obtained orphan drug designation from the US FDA for the treatment of advanced biliary tract cancer and soft tissue sarcoma.

Enlituo represents the first EGFR monoclonal antibody drug developed in China with independent intellectual property rights that are approved for the first-line treatment of mCRC. Classified as a 2.4 class modified biological new drug, cetuximab beta is prepared using a proprietary protein expression technique, effectively avoiding glycosylation modification that may lead to hypersensitivity.

As the second generation of 5-HT3 receptor antagonists, it have strong affinity to receptors and long time of drug action.

It is the first listed class I anti-tumor drug in the world, with patents from China and the United States. In addition, it has won the second prize of National Technological Invention Award and China Patent Gold Award, and has been listed in the National Medical Insurance Catalog since 2017.

Platinum-based agents exert the function by binding to DNAs to interfere with their replication, thereby preventing the division and growth of tumor cells. As a second-generation platinum-based agent, nedaplatin is more dissoluble in water and appears to be less toxic to the kidneys and the digestive system, and therefore more suitable for elderly patients as well as patients with renal insufficiency.

Pemetrexed is a multi-targeted anti-folate agent with low toxicity and broad-spectrum anti-tumor activity. Pemetrexed combined with platinum is a therapy recommended by CSCO guidelines for the first-line and maintenance treatment of advanced non-squamous NSCLC and advanced malignant pleural mesothelioma (MPM), which can significantly improve the efficacy of traditional chemotherapy and prolong the survival of patients.

As a cornerstone drug for the treatment of multiple myeloma, Bortezomib is used throughout the induction, consolidation and maintenance therapies for myeloma. In 2020, Bortezomib was recommended as a first-line drug for the full management of multiple myeloma in the Guidelines for Diagnosis and Treatment of Multiple Myeloma in China and was included in the NDRL.

The only bendamustine approved for indication of both CLL and B-cell NHL in China currently. In 2020, guidelines published by the Chinese Society of Clinical Oncology (CSCO) have recommended bendamustine as the first- and second- line treatment of multiple subtypes of B-cell lymphoma.

QUVIVIQ® (Daridorexant Hydrochloride Tablets) is an innovative dual orexin receptor antagonist (DORA) that overcomes the mechanistic limitations of traditional sedative-hypnotics. Since 2022, it has gained approval in multiple countries and regions including the United States, European Union, United Kingdom, Switzerland, Canada, Japan, and Hong Kong, China. In June 2025, driven by the collaboration between Simcere Pharmaceutical and Idorsia, it entered the Chinese market. As the only DORA-class drug approved by the European Medicines Agency (EMA) for improving daytime functioning, clinical trials confirm its rapid sleep induction, sustained sleep maintenance, significant improvement in daytime functioning, and favorable long-term safety profile. The approval of daridorexant in China offers a novel therapeutic option for insomnia patients, addressing unmet clinical needs unresolved by conventional sedative-hypnotics.

As a national class I innovative drug, Sanbexin^® can improve the neurological function of patients with strokes by inhibiting the dual mechanisms of oxidative stress damage and inflammatory damage. Sanbexin^® owns eight patents, with core patents authorized in the US, Japan and European countries and regions. It has received national special support for "Significant New Drug Development" and been awarded as one of “China’s Milestone Medical Achievements During the 13th Five-Year Plan Period”.

Expanded access policy of Sanbexin Sublingual Tablets in the US.pdf

It is the world’s first innovation drug in the field of stroke that has received US FDA BTD. Sanbexin® sublingual tablet is a dual-target brain cytoprotective agent composed of edaravone and dexborneol. These two active ingredients exert synergistic anti-oxidant and anti-inflammatory effects, which can significantly reduce brain cell damage caused by acute ischemic stroke.

Sublingual tablet is designed for quick disintegration under the tongue. This facilitates the active ingredients' rapid absorption into the blood and brain, bypasses the first-pass hepatic metabolism, which is conducive to higher drug bioavailability and faster onset of action. Sanbexin injections and sublingual tablets forms a combination that enables patients to receive a complete course of brain cytoprotection in and outside of the hospital during the acute phase of stroke.

As the first edaravone solution for injection marketed in China, BICUN^® is a representative pharmaceutical of free radical scavengers and anti-oxidant. It can improve the neurological function of stroke patients, and delay the progression and deterioration of amyotrophic lateral sclerosis.

Trazodone can relieve sleep disorders caused by SSRIs, and is often used as an adjunctive therapy for SSRIs. In addition, Trazodone can prolong the deep sleep, improve sleep quality, induce and maintain deep sleep, and alleviate anxiety and sexual dysfunction.

IREMOD^® is the first iguratimod approved for sale in the world and the only iguratimod approved for sale in China. It is also the only domestically-developed small molecule DMARD that was marketed over the past decade. IREMOD® has been recommended as the primary medication for treatment of active rheumatoid arthritis by multiple clinical practice guidelines and diagnosis criteria at home and abroad.

AIJIEWEI^® has passed consistency evaluation and entered the fourth national VBP. It blocks the JAK signal pathway by intracellular targeting and regulates various inflammatory factors associated with Ra, achieves potent and rapid improvement of traditional DMARDs in rheumatoid arthritis patients with poor efficacy, and is recommended by Chinese and International Authority RA guidelines.

With its unique sustained-release pellet technology, YINGTAIQING^® proves effective within one hour and the action can last up to 12 hours, ensuring fast and effective pain relief. It currently has both dosage forms of capsule and gel.

RUIFUSHU is the first nephrology product by Simcere, and has passed the consistency evaluation. It has been recommended by numerous domestic and international guidelines as the first-line treatment for preventing rejection following organ transplantation.

In December 2019, mycophenolate mofetil was approved for the treatment of class III-IV lupus nephritis of adult patients. This indication was included in the new National Reimbursement Drug List (NRDL), updated in March.

In addition, mycophenolate mofetil can also be used to treat other autoimmune diseases such as systemic lupus erythematosus (SLE), dermatomyositis, scleroderma, IgA nephropathy, membranous nephropathy (MN) and Nephrotic syndrome (NS).

As an exclusive production in the Chinese pharmaceutical market, OLMETEC PLUS^® is a new-generation compound preparation of an angiotensin II receptor blocker, olmesartan medoxomil, and a thiazide diuretic, hydrochlorothiazide. Developed and manufactured by Daiichi Sankyo, its commercialization right on the Chinese market is entitled to Simcere.

As a third-generation statin, it has been listed into a number of clinical practice guidelines in China as a recommended medication for dyslipidemia.

It is a long-lasting anti-hypertensive drug. It can be metabolized by the liver, and proves protective for the kidneys.

XINSHIPING is the second calcium channel blocker (CCB) that has adopted controlled release technology and passed the consistency evaluation in China. The drug is released at a uniform rate over 24 hours through the laser hole in the outer protective film of the tablet, avoiding the phenomenon where plasma concentration peaks and drops drastically, ensuring a stable and long-lasting hypotensive effect.

XIANNUOXIN is the first 3CL-targeting anti-COVID-19 innovative drug with independent intellectual property rights in China, which inhibits the 3CL protease necessary for SARS-CoV-2 viral replication, making the virus lose its ability to infect normal cells and spread. 

It is effective for all known COVID-19 mutants, with good overall safety.

Biapenem is a carbapenem antibiotic that can exert antibacterial effects by inhibiting the synthesis of bacterial cell walls, with broad-spectrum antibacterial activity against Gram-positive and Gram-negative aerobic and anaerobic bacteria. Biapenem is stable to human kidney dehydropeptidase-I (DHP-I) and can be administered alone without combination with DHP-I inhibitors.

Arbidol is a hemagglutinin fusion inhibitor and proves to be effective against viruses resistant to neuraminidase inhibitors. It is a broad-spectrum anti-viral agent for the treatment of influenza.

Amoxicillin mainly acts in the reproduction stage of microorganisms and inhibits the biosynthesis of cell wall mucopolypeptides. Potassium clavulanate can inactivate these enzymes produced by most bacteria by blocking the active site of β-lactamase. ANQI^® produced by our company has two dosage forms—tablets and granules.

Amoxicillin is a type of semi-synthetic penicillin β-lactam antibiotic. It has several dosage forms—capsules, dispersible tablets and granules.

It is the first Cefaclor suspension which has passed consistency evaluation for generic drugs in China, and is listed into the recommended medications by the Guidelines for the Treatment of Community-Acquired Pneumonia in China.

The Spleen-invigorating Bazhen Cake is made based on the recipe devised by Chen Shigong, a renowned imperial physician in the Ming Dynasty. As one of the classic recipes for strengthening the spleen and stomach, it was widely used and loved by the imperial members and the general public. This product in the form of a "cake" is developed by a team led by Nanjing University of Chinese Medicine. The sweet and fragrant product is convenient and safe to take as it is prepared with ingredients that are also used to make food, free of preservatives.

Qixuekang Oral Liquid nourishes and moisturizes your body to elevate qi and blood, thereby improving your complexion and sleep.Qixuekang Oral Liquid contains Panax notoginseng that invigorates and nourishes the blood, ginseng that supplements qi and soothes the nerves, Astragalus membranaceus that supplements qi and blood, and Kudzu root that transports nutrients and body fluid upwards. It improves insomnia, fatigue, lack of qi and blood, poor immunity, dry skin, dry mouth and tongue, dry cough, and other problems caused by insufficient nutrition in the upper body.

By physical action, BIQI^® montmorillonite powders can physically cover the surface of the gastrointestinal tract, and adsorb pathogenic factors, so as to quickly solve various diarrhea problems, without the need to enter the blood circulation, therefore being safe and non-toxic. Its prescription and preparation technique have obtained EU GMP certification and are now available in China and Europe.

This product is derived from Maxingshigan Decoction by Doctor Zhang Zhongjing. The Diagnosis and Treatment Protocol for COVID-19 (Trial Version 4) listed Maxingshigan Decoction as one of the recommended prescriptions.

The key to calcium supplementation is absorption, and the key to absorption is to ensure the absorbing of active vitamin D. The main ingredient of FANENG^® is active vitamin D, which is used to treat osteoporosis, and can effectively promote the absorption of calcium and reduce the incidence of hypercalcemia.

DING'AN^® hydrotalcite chewable tablets can quickly and effectively relieve a variety of discomfort symptoms in the stomach, and protect the gastric mucosa from damage.