創薬流通市場「薬市楽座」
安土桃山時代に自由取引市場として発展した「楽市楽座」にあやかり、創薬シーズ・技術のマーケットプラットフォームを創薬流通市場、「薬市楽座」と名付けました。このマーケットが楽市楽座のように発展することを願っています。
創薬流通市場である薬市楽座では、弊社がお預かりしている創薬シーズ・技術の情報をリストアップしています。ご興味に応じて検索していただくことが可能です。また、リストのダウンロードも行っていただけます。ご興味のあるものがあれば、お問い合わせボタンをクリックしていただき、弊社へのコンタクトをお願いいたします。追加情報を開示させていただきます。
なお、2019年6月27日より、日本語ページにおける、創薬シーズ、創薬技術の各リスト表記が英語に変更になりました。ダウンロード用のPDF、エクセルファイルは英語ページよりダウンロードできる資料と同一ですので、予めご了承下さいませ。
| 掲載日 | シーズ番号 | 作用機序 | 適応症 | 投与経路 | モダリティ | 開発ステージ | 備考 | |
|---|---|---|---|---|---|---|---|---|
| 20/04/08 | GEM167 | Elimination of MADD protein | Solid tumors | i.v., intra-tumoral | Gene therapy | Preclinical | A systemically deliverable oncolytic viral vector to target and eliminate the MADD protein overexpressed in a wide range of human cancer cell lines and involved in resistance. Systemic delivery demonstrated to colon, breast, liver, and ovarian tumors with no liver or kidney damage. Our parental vector infects and replicates only in cancer cells and has undergone extensive distribution and toxicity studies in mice and baboons and was previously approved for human trials. Breast, liver, and anaplastic thyroid cancer using siRNA achieved 41-60% TGI as mono or combo therapy. | 問合せ |
| 20/03/31 | GEM166 | Anti-Nodal antibody | Melanoma, Breast cancer, Pancreatic cancer and Hepatocellular carcinoma | i.v. | Antibody | Preclinical | The first anti-Nodal antibody drug targeting cancer stem cells and aggressive tumors. Nodal is a secreted protein in the embryo. The expression is lost in most adult tissues, but is reactivated in aggressive tumor cells. Expression level is highly correlated with invasion, metastasis, drug resistance and cancer prognosis. Combination of anti-Nodal Ab with current therapies is more effective than monotherapy. A companion diagnostic Nodal ELISA kit is also being developed which can be used as a biomarker for patient selection and disease monitoring. |
問合せ |
| 20/03/25 | GEM035 | An anti-ENO1 antibody | Immune diseases, various cancers | s.c. | Protein | US FDA IND cleared | GEM035 is a humanized antibody against unique ENO1 target. This therapeutic antibody is first-in-class to target inflammatory macrophage and demonstrates efficacy in animal models of MS, IPF, and IBD. It also showed efficacy in animal models of lung, pancreatic, and prostate cancer, most likely by targeting tumor associated macrophage (TAM). GEM035 may be developed for treatment of COVID-19 induced ARDS based on its capability to suppress macrophage related immune response. GEM035 has a worldwide patent protection. US IND of GEM035 is approved and active now for treating MS. | 問合せ |
| 20/03/11 | GEM164 | Anthracycline topoisomerase II inhibitor | Breast cancer, Bladder cancer, Kaposi's sarcoma, lymphoma, and Acute lymphocytic leukemia | i.v. | Small molecule | Bioequivalence study completed | Generic pegylated liposomal doxorubicin hydrochloride. Doxorubicin is well known to cause cardiotoxicity and develop congestive heart failure. Cardiotoxicity of GEM164 is expected to be substantially lower than non-liposomal doxorubicin. Bioequivalence with CAELYX has been demonstrated. |
問合せ |
| 20/03/02 | GEM163 | Reduction of virus-replication and reduction of inflammation | Virus diseases （incl. coronaviruses）** | Oral | Oligo-saccharides | NDIN** ready | A novel, intestinally absorbable derivative (pat. pend.) of GRAS αCD (α-cyclodextrin) to reduce virus entry (endocytosis) and replication/assembly of virueses (availability of lyso-phospholipids). βCDs have been effective in vitro against many virus infections, incl. coronaviruses, and topically against influenza and HSV2. αCDs avoid the ototoxicity of βCDs and were more effective (tested in HIV-1 cells). **New dietary ingredient notification as a nutritional supplement/FSMP |
問合せ |
| 20/03/02 | GEM162 | Restoration of autophagy and reduction of inflammation | Age-related diseases** | Oral | Oligo-saccharides | NDIN** ready | A novel, intestinally absorbable derivative (pat. pend.) of GRAS αCD (α-cyclodextrin) as an intermittent fasting mimetic. βCDs have been effective in vivo against many age-related diseases, including cancer, AD, and PD. αCDs are more effective against endocytosis than βCDs and lack the βCDs' ototoxicity. In the EU, oral αCD may claim to "reduce post-prandial glycemic response", but has low and variable bioavailability. **New dietary ingredient notification as a nutritional supplement/FSMP |
問合せ |
| 20/03/02 | GEM161 | Restoration of autophagy and reduction of inflammation | Cardiovascular and Metabolic Diseases | Oral | Oligo-saccharides | Phase 2b/3 ready | A novel derivative (pat. pend.) of hydroxypropyl-α-cyclodextrin (HPαCD) that down-regulates the PI-system by controlling serum phospholipids and, thereby, reduces endocytosis. βCDs have been shown to be effective in vivo against atherosclerosis (AS), NAFLD, but can cause permanent hearing loss (not applicable to αCDs). Oral αCD is clinically effective against metabolic syndrom, but has low and variable bioavailability. 505(b)(2) is applicable. | 問合せ |
| 20/03/02 | GEM160 | Restoration of autophagy and reduction of inflammation | Neuro-degenerative diseases | Oral, Intra-thecal | Oligo-saccharides | Phase 2b/3 ready | A novel derivative (pat. pend.) of hydroxypropyl-α-cyclodextrin (HPαCD) that down-regulates serum phospholipids and prevents aging cells from accumulating Aβ/tau (AD), α-syn (PD), myelin (MS), mHTT (HD), SOD1 (ALS), ... . βCDs were effective in vivo against AD and PD, but development was abandoned (except for NPC) due to the risk of permanent hearing loss (not applicable to αCDs). In the US, αCD is generaly recognized as safe (GRAS) for oral use; in the EU, αCDs are approved for oral and parenteral use. 505(b)(2) is applicable. | 問合せ |
| 20/03/02 | GEM159 | Restoration of autophagy and reduction of inflammation | Breast cancer and other carcinomas* | Oral, intra-venous | Oligo-saccharides | Phase 2b/3 ready | A novel intestinally absolrbable derivative (pat. pend.) of hydroxypropyl-α-cyclodextrin (HPαCD) that down-regulates the Phosphoinositide-system by controlling serum phospholipids and, thereby, reduces endocytosis. βCDs were effective in vivo against breast, ovarian, lung, and colon cancer, and metastatic melanoma, but need to be infused overnight and can cause permanent hearing loss. αCDs are not ototoxic and were more effective in vivo against growth and metastases of breast cancer. *Mono- or adjuvant treatment. 505(b)(2) is applicable. |
問合せ |
| 20/02/27 | GEM158 | Anti-mitotic chemotherapy | Small cell lung cancer | i.v. | Small molecule | Phase 1 completed | Proprietary innovative albumin-stabilized pegylated liposomal docetaxel formulation. Elevated exposures of docetaxel compared with free (nonencapsulated) docetaxel were confirmed in animals and humans. Acceptable tolerability and results suggesting anti-tumor efficacy were observed in Phase 1. FDA orphan drug designation was granted and confirmed with FDA that 505(b)(2) NDA pathway appears to be an acceptable approach. | 問合せ |