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Colorectal cancer (CRC) is the leading cause of cancer death; however, targets with broad anti-CRC effects are limited. Sirtuin6 (SIRT6) is a conserved nicotinamide adenine dinucleotide (NAD+)-dependent deacetylase that is widely pathologically downregulated in CRC. MDL-811, an allosteric SIRT6 activator, enhances SIRT6 deacetylation. Pharmacokinetic studies were performed by Shanghai Medicilon Inc, China, following standard protocols.

Gastric cancer (GC) is one of the most common malignancies and is the leading global cause of death by cancer. Over recent decades, targeted therapies and immunotherapy have become significant new approaches for the treatment of GC. Ferroptosis is a newly verified form of modulated cell death that is characterized by lipid peroxidation. Further exploration of the function of ferroptosis in the progression of GC has provided novel opportunities for diagnosis and treatment. The overexpression of MGST1 induced the activation of the Akt/GSK-3β pathway. An Akt inhibitor antagonized the inhibitory effects of MGST1 on autophagy and ferroptosis. MGST1 and ATG16L1 overexpression, and MGST1 depletion assay were conducted by Medicilon.

Cell division cycle 7 (CDC7), a serine/threonine kinase, plays important roles in the initiation of DNA replication. TAK-931, a highly specific CDC7 inhibitor, acts as a next-generation of replication stress (RS) inducer. Combination treatment with TAK-931 and immune checkpoint inhibitors (ICIs) enhances antiproliferative activities in preclinical syngeneic mouse models. The flowcytometry (FCM)-based immune profiling panel studies in J558 allograft syngeneic mouse models were performed at Medicilon. In vivo efficacy studies in J558 allograft models in combination with anti-mPD-1, anti-mPD-L1, and anti-mCTLA-4 antibodies were performed at Medicilon. Therapeutic potential of TAK-931 in antitumor efficacy and immunity, which may improve clinical benefit of the currently-used immunotherapy by combination treatment.

Chrysin is a natural flavonoid that has been reported as a potential treatment for non-alcoholic fatty liver disease (NAFLD). Researchers synthesized a novel chrysin derivative prodrug (C-1) and further investigated its potential therapeutic mechanism against NAFLD in vitro and in vivo. C-1 had a low toxicity profile. Their data demonstrated that C-1 may be a promising agent for NAFLD therapy. Evaluation experiments of the acute toxicities of C-1 were conducted by Medicilon.

美迪西作為核新生物的合作伙伴，為XY003的臨床前研發(fā)提供了CMC研究（包括原料藥和制劑）服務(wù)，并獲頒“2024年度杰出合作伙伴獎”和感謝信，其高效研發(fā)服務(wù)和專業(yè)創(chuàng)新能力獲核新生物高度肯定。

美迪西作為海擘生物合作伙伴，為NC527-X提供了CMC研發(fā)（原料藥、制劑）、臨床前研發(fā)（藥效、藥代、安評）以及注冊申報等一站式臨床前綜合研發(fā)服務(wù)。這也是美迪西又一個提供全套IND申報服務(wù)的成功案例！

美迪西作為銀珠醫(yī)藥的合作伙伴，依托肺癌骨轉(zhuǎn)移模型藥效評價模型，為小分子免疫抑制劑YZ008的研發(fā)提供了藥效服務(wù)，加速了新藥研發(fā)進程，為此次合作奠定了堅實基礎(chǔ)。

作為寶太生物的戰(zhàn)略合作伙伴，上海美迪西生物醫(yī)藥股份有限公司為BIOT-006的研發(fā)提供了從藥物發(fā)現(xiàn)到IND申報的一站式臨床前綜合研發(fā)服務(wù)。這是繼美迪西一站式助力寶太生物BIOT-001獲中美雙報雙批后，雙方合作達成的又一重要里程碑。

上海美迪西生物醫(yī)藥股份有限公司作為恒瑞醫(yī)藥的戰(zhàn)略合作伙伴，為HRS-5817注射液的研發(fā)提供了藥代動力學(xué)研究和符合GLP規(guī)范的安全性評價服務(wù)（僅用時5個月），以高效、高質(zhì)的研發(fā)服務(wù)推動HRS-5817注射液快速獲批臨床。自從美迪西與恒瑞就新分子藥物（ADC/小核酸/CGT）達成臨床前評價戰(zhàn)略合作以來，這已是繼HRS-9563注射液后，雙方合作取得的又一重要里程碑。

作為慕恩生物的合作伙伴，美迪西依托符合中美雙報標(biāo)準(zhǔn)的GLP體系以及高效的臨床前研究服務(wù)平臺，為MNO-863提供了涵蓋急毒、長毒、安全藥理等研究服務(wù)，為中美雙批奠定堅實基礎(chǔ)。