| Biotech | Pharma Company | Type/Product Area | Amount | Terms/Details (Month) |
| Company** | (Symbol/Country) | |||
| (Country) | ||||
| Abgenix Inc. | Schering-Plough | Collaborative research | ND | Schering-Plough has option to |
| (subsidiary of | Research Institute | agreement; use of Abgenix's | enter research and license agree- | |
| Cell Genesys Inc.) | (unit of Schering- | XenoMouse technology | ment under which Abgenix would | |
| Plough Corp.; | to generate fully human | get additional research and mile- | ||
| NYSE:SGP) | monoclonal antibodies to | stone payments as well as royalties | ||
| an undisclosed Schering- | (2/98) | |||
| Plough target antigen | ||||
| Advanced Polymer | Pharmacia & | Agreement to use | ND | Pharmacia & Upjohn will fund all |
| Systems Inc. | Upjohn Inc. | Advanced Polymer's | product development, conduct | |
| (NYSE:PNU; U.K.) | Microsponge system to | clinical trials and commercialize | ||
| develop a topical formula- | product worldwide; Advanced | |||
| tion of one of Pharmacia | Polymer gets R&D funds, license | |||
| & Upjohn's therapeutics | fees, milestones and royalties (1/98) | |||
| Alkermes Inc. | The R.W. Johnson | Agreement to develop | $30M | Alkermes gets $30M in develop- |
| Pharmaceutical | injectable, sustained- | ment funds and milestones; John- | ||
| Research Institute | release formulation of | son & Johnson gets worldwide | ||
| (unit of Johnson | erythropoietin via | commercial rights; Alkermes gets | ||
| & Johnson; NYSE:JNJ) | Alkermes' ProLease | milestones; Alkermes will manu- | ||
| drug delivery technology; | facture commercial product; John- | |||
| product for use in non- | son & Johnson will conduct clini- | |||
| dialysis indications to | cal trials and get regulatory appro- | |||
| restore blood cell levels | vals (1/98) | |||
| in kidney patients | ||||
| Alza Corp. | Janssen Pharma- | Collaborative agreement | ND | Alza will fund product develop- |
| ceutica NV | to use Alza's E-Trans | ment for next 2 years; Janssen has | ||
| (Belgium; unit | drug delivery technology | limited option to fund development | ||
| of Johnson & | (uses electric current to | after that point; if it exercises option, | ||
| Johnson; NYSE:JNJ) | administer drug through | Janssen will market product and | ||
| the skin) with a fentanyl | Alza will share profits in U.S. and | |||
| drug product for | get royalties elsewhere; Alza has | |||
| treating chronic pain | right to copromote in U.S.; if Janssen | |||
| does not exercise option, Alza retains | ||||
| all rights to develop and commercial- | ||||
| ize product worldwide (1/98) | ||||
| Bio-Technology | Swiss Serum and | Development and | ND | Agreement covers scale-up and |
| General Corp. | Vaccine Institute | licensing agreement on | optimization of vaccine manufac- | |
| (Switzerland) | Bio-Technology Gen- | turing process as well as clinical | ||
| eral's 3rd-generation | development, registration and | |||
| recombinant hepatitis | marketing of product; companies | |||
| B virus vaccine (viral | also will develop combination | |||
| surface antigens S, | vaccines; Swiss Serum will buy | |||
| pre-S1 and pre-S2 | vaccine from Bio-Technology | |||
| expressed in mamma- | General and distribute in western | |||
| lian cells) | Europe, Latin America and other | |||
| countries; Bio-Technology General | ||||
| gets milestones and royalties (2/98) | ||||
| Cantab | Kaketsuken | Research and option | ND | Kaketsuken will fund research at |
| Pharmaceuticals | (Japan) | agreement to develop | Cantab for 2 years in return for | |
| plc (U.K.) | Cantab's DISC VSV | option to license all product rights | ||
| virus (genetically | for Japan and certain other Asian | |||
| disabled live Varicella | territories; once research phase is | |||
| zoster virus) as pro- | completed, parties will form devel- | |||
| phylactic vaccine for | opment and marketing agreement, | |||
| chickenpox and shingles | under which Cantab will get license | |||
| and milestone fees and royalties and | ||||
| retain marketing and sublicensing | ||||
| rights for rest of world (1/98) | ||||
| Chiron Corp. | Pharmacia & | Strategic collaboration | ND | Chiron gets up-front payment; |
| Upjohn Inc. | to identify small mole- | companies will contribute equal | ||
| (NYSE:PNU; U.K.) | cule inhibitors of | resources and funding for all | ||
| hepatitis C virus (HCV) | phases of product development; | |||
| companies will share worldwide | ||||
| marketing rights; Chiron will pro- | ||||
| vide its scientific expertise on | ||||
| HCV and nonexclusive rights to | ||||
| all HCV targets covered by its | ||||
| patents and patent applications | ||||
| (2/98) | ||||
| Chiroscience | Bristol-Myers | Research and licensing | ND | 3-year agreement; Bristol-Myers |
| Group plc (U.K.) | Squibb Co. | agreements on use of | gets worldwide license on D2163 | |
| (NYSE:BMY) | matrix metalloproteinase | and D1927; Chiroscience gets | ||
| (MMP) inhibitors for | access fees, research funds, mile- | |||
| treating cancer; includes | stone payments and royalties; | |||
| Chiroscience's 2nd-gen- | Bristol-Myers gets all rights to new | |||
| eration oral compounds | and jointly selected MMP inhib- | |||
| D2163 (currently in U.K. | itors that are developed for oncol- | |||
| Phase I trials) and D1927; | ogy; Chiroscience retains rights | |||
| also covers discovery of | in all other therapeutic areas (2/98) | |||
| new MMP inhibitors via | ||||
| Chiroscience's gene | ||||
| expression technology | ||||
| Chrysalis | OrthoLogic Corp. | Option on license for | $0.8M | OrthoLogic acquired minority |
| BioTechnology | (NASDAQ:OLGC) | Chrysalis' synthetic | (equity; | equity stake in Chrysalis for $0.75M; |
| Inc.* | 23-amino-acid-peptide | % ND) | OrthoLogic has 9-month option on | |
| chrysalin for orthopedic | worldwide exclusive license to ortho- | |||
| applications, initially | pedic applications of chrysalin; Ortho- | |||
| for healing of fractures | Logic can continue and expand option | |||
| contingent on preclinical results; | ||||
| OrthoLogic will fund R&D, mile- | ||||
| stones and clinical trials (1/98) | ||||
| Chrysalis | Pfizer Inc. | Genomics-based trans- | ND | Chrysalis will use its high-capacity |
| International Corp. | (NYSE:PFE) | genic research contract | transgenic animal capabilities to | |
| and its wholly owned | and collaboration to | identify and validate new thera- | ||
| subsidiary, | identify and validate new | peutic targets from genetic data | ||
| Chrysalis DNX | therapeutic targets for 2 | generated by Pfizer's genomics | ||
| Transgenic | major disease categories | initiative; Pfizer will fund research | ||
| Sciences | via Chrysalis' transgenic | for 2 years (1/98) | ||
| mouse and rat lines | ||||
| CytoMed Inc.* | UCB Pharma | Research collaboration | ND | UCB will fund joint research pro- |
| (division of UCB | on therapeutics for | gram; further details ND (3/98) | ||
| Group; Belgium) | major inflammatory | |||
| diseases (via small | ||||
| molecules that modulate | ||||
| specific anti-inflam- | ||||
| matory activities) | ||||
| deCode Genetics | F. Hoffmann- | Collaboration to dis- | $200M | 5-year collaboration; deCode gets |
| Inc.* (Iceland) | La Roche Ltd. | cover disease genes | (equity; | up to $200M (including equity |
| (Switzerland) | for use in therapeutics | % ND) | investment, research funds and | |
| and diagnostics; use of | milestone payments); Roche gets | |||
| Icelandic population data- | rights to develop small molecule | |||
| base to discover genes | drugs and drugs based on gene | |||
| that predispose people | products as well as diagnostics; | |||
| to developing 12 | deCode retains rights to gene and | |||
| common diseases | antisense therapies (2/98) | |||
| (4 cardiovascular; 4 | ||||
| psychiatric/neurologic; | ||||
| 4 metabolic); collab- | ||||
| oration also includes | ||||
| pharmacogenomics | ||||
| component | ||||
| DepoMed Inc. | The R.W. Johnson | Research collaboration | ND | ND (3/98) |
| Pharmaceutical | on use of DepoMed's | |||
| Research Institute | Gastric Retention Sys- | |||
| (unit of Johnson & | tem (orally administered, | |||
| Johnson; NYSE:JNJ) | controlled-release system) | |||
| with a Johnson & Johnson | ||||
| drug | ||||
| Elan | Novartis Pharma- | Development and | $18M | Elan will reformulate Novartis' |
| Pharmaceutical | ceuticals Corp. | licensing agreement on | drug and test its pharmacokinetics | |
| Technologies | (unit of Novartis | use of Elan's extended- | in human trials; Novartis will con- | |
| (division of Elan | AG; Switzerland) | release drug delivery | duct all other clinical trials and | |
| Corp. plc; Ireland) | technology with a | product registrations; Elan gets | ||
| Novartis prescription | development and licensing fees of | |||
| drug (not disclosed) | $18M total, as well as royalties; | |||
| Elan will manufacture product for | ||||
| Novartis and gets manufacturing | ||||
| fees (1/98) | ||||
| Solvay Pharma- | Agreement on use of | ND | Elan will develop new dosage | |
| ceuticals Inc. | Elan's extended-release | formulation of Luvox; Solvay will | ||
| (member of | drug delivery technology | conduct all clinical trials and pro- | ||
| The Solvay Group; | with Solvay's prescrip- | duct registrations; Elan gets dev- | ||
| Belgium) | tion drug Luvox (flu- | elopment and licensing fees as | ||
| voxamine; a selective | well as milestones; Elan will manu- | |||
| serotonin reuptake | facture new formulation and gets | |||
| inhibitor for treating | manufacturing fees; Elan also gets | |||
| obsessive compulsive | royalties (2/98) | |||
| disorder and depression) | ||||
| Epix Medical Inc. | Mallinckrodt Inc. | Collaboration to improve | ND | Companies will develop hardware |
| (NYSE:MKG) and | and expand capabilities | and software to be used with Epix's | ||
| General Electric | of magnetic resonance | MS-325 injectable contrast agent; | ||
| Medical Systems | imaging for diagnosing | financial details ND (1/98) | ||
| (NYSE:GE) | coronary artery disease | |||
| and peripheral vascular | ||||
| disease | ||||
| Ergo Science | The R.W. Johnson | Collaboration to | $40M | Ergo gets $10M license fee plus |
| Corp. | Pharmaceutical | develop Ergoset | (equity; | $10M equity investment; Ergo |
| Research Institute | (bromocriptine mes- | % ND) | also gets $20M on FDA approval | |
| and Ortho-McNeil | ylate, dopamine agonist) | of Ergoset for Type II diabetes; | ||
| Pharmaceutical Inc. | and other products as | companies will share equally costs | ||
| (units of Johnson | treatments for Type II | of developing and commercializ- | ||
| & Johnson; NYSE:JNJ) | diabetes and obesity | ing Ergoset and other products; | ||
| (NDA accepted for | they also will share profits equally; | |||
| filing 10/97) | Ergo gets royalties on sales outside | |||
| U.S.; Ergo gets additional mile- | ||||
| stones for other products; agree- | ||||
| ment subject to antitrust consider- | ||||
| ations (2/98) | ||||
| Gene Logic Inc. | NV Organon (unit | Gene expression data- | ND | 3-year agreement; Organon gets |
| of Akzo Nobel; | base alliance; use of | nonexclusive access to database | ||
| the Netherlands) | Gene Logic's Normal | and bioinformatics system for use | ||
| database (reference set | in its internal drug discovery pro- | |||
| of quantitative gene | gram; Gene Logic also will con- | |||
| expression profiles in | struct gene expression database | |||
| mouse, rat and human | exclusively for Organon; Organon | |||
| tissues) and its bio- | responsible for worldwide devel- | |||
| informatics system for | opment and commercialization of | |||
| analysis and integration | therapeutics; Gene Logic retains | |||
| of gene expression data | rights to diagnostics and certain | |||
| therapeutics; Gene Logic gets | ||||
| research funds, license fees, mile- | ||||
| stones and royalties (1/98) | ||||
| Genentech Inc. | Dako A/S | Agreement to develop | ND | Dako gets license to develop |
| (Denmark) | in vitro diagnostic kit | immunohistochemical diagnostic | ||
| for screening breast | kit; Genentech gets royalties; | |||
| cancer patients for | further details ND (3/98) | |||
| overexpression of | ||||
| HER2 (growth factor | ||||
| receptor) and to identify | ||||
| their potential eligibility | ||||
| to be treated with | ||||
| Herceptin (humanized | ||||
| anti-HER2 monoclonal | ||||
| antibody; Phase III trials | ||||
| completed) | ||||
| Genentech Inc. | Pharmacia & | Development and | $35M | Pharmacia & Upjohn gets exclu- |
| Upjohn Inc. | licensing agreement on | sive worldwide rights to TPO; | ||
| (NYSE:PNU; U.K.) | Genentech's thrombo- | companies will jointly develop | ||
| poietin (TPO) for treat- | product; Genentech will manufac- | |||
| ing thrombocytopenia | ture product for development | |||
| in cancer patients | work and commercialization; | |||
| receiving chemotherapy | Pharmacia & Upjohn will fund | |||
| and in stem cell trans- | future development costs and pay | |||
| plants (currently in | $35M in license fees through | |||
| Phase II trials) | 2000 (including initial $12M fee); | |||
| if product approved for market- | ||||
| ing, Genentech gets final transfer | ||||
| payment and royalties; Genentech | ||||
| will conduct clinical trials in myelo- | ||||
| ablative therapy; Pharmacia & | ||||
| Upjohn will conduct clinical trials | ||||
| for all other indications (1/98) | ||||
| Genzyme | Merck & Co. Inc. | License agreement on | $8M | Merck gets nonexclusive rights to |
| Molecular | (NYSE:MRK) | Genzyme Molecular's | cancer assay methods; Genzyme | |
| Oncology | methods for screening | Molecular gets up-front payment | ||
| (division of | small molecule com- | and $8M in milestones, as well as | ||
| Genzyme Corp.) | pounds that inhibit | royalties on sales of any thera- | ||
| binding of cancer- | peutic products (2/98) | |||
| related protein MDM2 | ||||
| to the p53 protein | ||||
| (binding prevents p53 | ||||
| from activating genes | ||||
| that control cell | ||||
| division) | ||||
| Schering-Plough | Research and option | $80M | Schering-Plough has option to | |
| Corp. (NYSE:SGP) | agreement; use of | exclusively license Genzyme Mol- | ||
| Genzyme Molecular's | ecular's gene delivery systems for | |||
| lipid gene delivery | use with 6 of its genes; if it exer- | |||
| systems with several of | cises option, Genzyme Molecular | |||
| Schering-Plough's genes, | gets license fees, research funding | |||
| including p53 tumor | and milestones totaling $80M; | |||
| suppressor gene, to | Genzyme Molecular gets $7M | |||
| develop gene therapy | over next year for research on p53 | |||
| products | gene therapy product (1st of 6 | |||
| genes); Genzyme Molecular also | ||||
| gets royalties on sales (1/98) | ||||
| Immusol Inc.* | Pfizer Inc. | Genomic-based research | ND | Immusol will design specific |
| (NYSE:PFE) | collaboration to validate | ribozymes for each candidate gene | ||
| therapeutic targets in | target sequence of Pfizer; further | |||
| Pfizer's pipeline via | details ND (3/98) | |||
| Immusol's hairpin | ||||
| ribozyme technology | ||||
| and in vivo assay model | ||||
| to determine gene func- | ||||
| tion in human cell lines | ||||
| Inhale Therapeutic | Eli Lilly and Co. | Collaboration on use | $20M | Inhale gets $20M in R&D funds |
| Systems | (NYSE:LLY) | of Inhale's deep-lung | and milestones; Lilly gets world- | |
| delivery system for | wide rights to formulated drug; | |||
| macromolecules to | Inhale gets royalties; Inhale will | |||
| formulate an unspeci- | manufacture packaged powders | |||
| fied protein drug for | for and supply inhalation devices | |||
| Lilly | to Lilly; Lilly responsible for clini- | |||
| cal trials, product registration and | ||||
| marketing (1/98) | ||||
| Integra | Johnson & Johnson | Strategic alliance on | $12M | Integra gets $12M in milestones; |
| LifeSciences Corp. | Professional Inc. | an absorbable, collagen- | Johnson & Johnson will fund all | |
| (subsidiary of | based implant (combined | development costs beyond pre- | ||
| Johnson & Johnson; | with an RGD peptide) for | clinical stage; Integra will manu- | ||
| NYSE:JNJ) | repairing and regenerating | facture product; Johnson & John- | ||
| articular cartilage | son will develop arthroscopic | |||
| instrumentation to be used in | ||||
| surgeries; Johnson & Johnson gets | ||||
| worldwide marketing rights (2/98) | ||||
| Intercardia Inc. | Opocrin SpA | Letter of intent to | ND | Intercardia will get worldwide |
| (Italy) | license OP2000 (an | license except in Japan and | ||
| oligosaccharide product | South Korea; Intercardia will | |||
| derived from heparin | conduct clinical trials; Opocrin | |||
| with antithrombotic and | will get $1M on signing of defin- | |||
| anti-inflammatory pro- | itive agreement (3/98) | |||
| perties) for treating | ||||
| inflammatory bowel | ||||
| disease | ||||
| Ligand | SmithKline | Collaboration on small | $9M | SmithKline will buy 0.27M shares |
| Pharmaceuticals | Beecham plc | molecule drugs that | (equity; | Ligand common stock for $5M |
| Inc. | (NYSE:SBH; U.K.) | modulate signaling | % ND) | ($18.22/share, premium to market) |
| pathway controlled by | and will also pay $1M for a 5- | |||
| leptin; use of Ligand's | year warrant to buy 0.15M shares | |||
| STATS technology | at $20/each; SmithKline will buy | |||
| (signal transduction and | more stock on achievement of one | |||
| activator of transcription) | specific milestone and will pay | |||
| to develop oral drugs | cash for subsequent milestones; | |||
| for treating or prevent- | SmithKline gets exclusive world- | |||
| ing obesity | wide rights to products; Ligand | |||
| gets royalties; subject to anti- | ||||
| trust considerations (3/98) | ||||
| Magainin | Ambalal Sarabhai | Memorandum of under- | ND | Magainin will license applicable |
| Pharmaceuticals | Enterprises Ltd. | standing to form a joint | technology to the joint venture and | |
| Inc. | (India) | venture in India to | provide technical assistance; | |
| develop and commer- | Sarabhai will conduct and fund all | |||
| cialize certain magainin | development and commercializa- | |||
| peptide compounds | tion activities for the joint venture; | |||
| (including Cytolex | Magainin and Sarabhai will share | |||
| [a.k.a. MSI-78]) for | profits equally (1/98) | |||
| treating infection in | ||||
| diabetic foot ulcers as | ||||
| well as other indications | ||||
| Medarex Inc. | Schering AG | Research collaboration | $9M | Medarex gets R&D payments, |
| (Germany) | and license agreement; | license fee and milestones totaling | ||
| use of Medarex' HuMAb- | $9M, plus royalties (2/98) | |||
| mouse technology to | ||||
| make fully human mono- | ||||
| clonal antibodies to a | ||||
| Schering antigen | ||||
| Molecular | Rhone-Poulenc | DNA microarray tech- | ND | Rhone-Poulenc Rorer will provide |
| Dynamics Inc. | Rorer Inc. (sub- | nology access agreement; | funding and technical expertise; | |
| and Amersham | sidiary of Rhone- | collaboration for contin- | it gains early access to integrated | |
| Pharmacia | Poulenc SA; NYSE: | ued development of new | microarray systems; further details | |
| Biotech (Sweden) | RP; France) | microarray technologies | ND (1/98) | |
| NanoSystems | Boehringer | Development, license | ND | NanoSystems gets up-front license |
| LLC* | Ingelheim GmbH | and supply agreement; | fee, milestone payments and | |
| (Germany) | use of NanoCrystal | royalties; further terms ND (2/98) | ||
| technology (improves | ||||
| delivery of poorly | ||||
| water-soluble drugs) | ||||
| for undisclosed com- | ||||
| pound for respiratory | ||||
| delivery | ||||
| Oncor Inc. | Becton Dickinson | Licensing agreement | ND | Oncor gets license fees, research |
| & Co. (NYSE:BD) | for Oncor's Sunrise | funding, milestones and royalties | ||
| Detection System; to | (3/98) | |||
| be used in conjunction | ||||
| with Becton's Strand | ||||
| Displacement Ampli- | ||||
| fication technology | ||||
| in kits for infectious | ||||
| disease detection | ||||
| OncorMed Inc. | Schering-Plough | OncorMed will provide | ND | OncorMed will analyze patient |
| Research Institute | p53 pharmacogenomic | samples (to identify those with | ||
| (unit of Schering- | services for Schering- | missing or defective p53 gene) for | ||
| Plough Corp.; | Plough's clinical trials | Schering-Plough's clinical trials; | ||
| NYSE:SGP) | of its rAd/p53 cancer | OncorMed also will provide se- | ||
| gene therapy (to ascertain | quencing and other services (1/98) | |||
| p53 status of prospective | ||||
| clinical trial subjects) | ||||
| Oxford Asymmetry | Bayer AG | Development of lead | $26M | 2-year collaboration; Bayer will |
| International plc | (Germany) | discovery libraries of | screen Oxford's libraries for leads; | |
| (LSE:OAI; U.K.) | new chemical entities | Oxford gets $14.6M over 2 years, | ||
| (via Oxford's combi- | plus $11.4M in milestones for | |||
| natorial chemistry) as | each product that completes clini- | |||
| product candidates for | cal trials; Oxford also gets royal- | |||
| Bayer's pharmaceutical, | ties (2/98) | |||
| animal health and crop | ||||
| protection businesses | ||||
| Oxford Biomedica | Rhone-Poulenc | Feasibility study on | ND | ND (1/98) |
| plc (LSE:OXB; U.K.) | Rorer Inc. (sub- | use of Oxford's lenti- | ||
| sidiary of Rhone- | viral vector systems | |||
| Poulenc SA; NYSE: | in Rhone-Poulenc | |||
| RP; France) | Rorer's functional | |||
| genomics program (to | ||||
| transfer genes to certain | ||||
| non-dividing tissues) | ||||
| PowderJect | Glaxo Wellcome | Collaboration, develop- | $321M | Glaxo gets exclusive worldwide |
| Pharmaceuticals | plc (NYSE:GLX; U.K.) | ment, license and option | (7.7% | rights to use PowderJect technol- |
| plc (U.K.) | agreement on DNA vac- | equity) | ogy to commercialize prophylac- | |
| cines using PowderJect | tic HBV vaccine and options | |||
| technology (includes pro- | on others; Glaxo will take over | |||
| phylactic hepatitis B | development of prophylactic HBV | |||
| virus (HBV) DNA vac- | vaccine, for which it will pay $4M | |||
| cine, HBV and HIV DNA | license fee; Glaxo also will buy | |||
| vaccines, DNA vaccines | $20M of equity (4.9M shares for | |||
| for 2 infectious diseases | a 7.71% stake) and pay another | |||
| and others); technology | $297M in milestones, research | |||
| based on DNA-coated | funding and license fees as it exer- | |||
| gold particles delivered | cises its options on the other vac- | |||
| via needleless injection | cines; Glaxo will be responsible | |||
| (prophylactic HBV | for all vaccine development and | |||
| vaccine in clinical trials) | commercialization; PowderJect | |||
| gets royalties; PowderJect will | ||||
| manufacture and supply its device; | ||||
| 5-year agreement subject to anti- | ||||
| trust considerations (3/98) | ||||
| Progenics | Roche Discovery | Collaboration on orally | ND | Roche gets exclusive worldwide |
| Pharmaceuticals | Welwyn (U.K.; | active drugs that target | license to Progenics' HIV co- | |
| Inc. | member of The | HIV coreceptors CCR5 | receptor technology; Progenics | |
| Roche Group; | and CD4 (required for | gets up-front and milestone pay- | ||
| Switzerland) | fusion and infection of | ments, research funding for 3 | ||
| immune cells) | years and royalties (1/98) | |||
| Protein Design | Eli Lilly and Co. | Collaborative agree- | $15M | Protein Design got $3M in initial |
| Labs Inc. | (NYSE:LLY) | ment on antibiotics | fee and gets annual research fund- | |
| for treating certain | ing of $2.4M for 5 years; Protein | |||
| bacterial infections, | Design also gets milestones and | |||
| including those caused | royalties; Lilly gets exclusive | |||
| by antibiotic-resistant | worldwide rights to gene targets | |||
| strains; use of high- | and human pharmaceutical and | |||
| throughput screens | related diagnostic products directed | |||
| and combinatorial | to 7 specific genera of bacteria; | |||
| chemistry to identify | Protein Design retains rights to | |||
| bacterial genes that | targets and compounds related to | |||
| are differentially ex- | other bacteria, viruses and fungi; | |||
| pressed during infection | parties will negotiate copromotion | |||
| rights in U.S. and Canada (1/98) | ||||
| RiboGene Inc.* | Dainippon | Collaboration on anti- | $8M | Dainippon gets exclusive world- |
| Pharmaceutical | bacterial compounds | (equity; | wide rights to develop and market | |
| Co. Ltd. (Japan) | that inhibit or interfere | % ND) | products; RiboGene gets $2M | |
| with protein translation | annually for 3 years to fund | |||
| in pathogenic bacteria | research; Dainippon also will buy | |||
| (will use 2 of Ribo- | $2M in RiboGene equity; Ribo- | |||
| Gene's principal bacterial | Gene gets milestone payments for | |||
| targets) | each compound, as well as royal- | |||
| ties; RiboGene has right to copro- | ||||
| mote products in Europe and U.S.; | ||||
| RiboGene retains rights to its | ||||
| other bacterial targets (1/98) | ||||
| Sepracor Inc. | Janssen Pharma- | Collaboration and | ND | Companies will jointly fund prod- |
| ceutica NV | license agreement on | uct development; Janssen has op- | ||
| (Belgium; unit | 3rd-generation non- | tion to acquire certain rights in U.S. | ||
| of Johnson & | sedating antihistamine | and elsewhere; if exercised, com- | ||
| Johnson; NYSE:JNJ) | norastemizole (for treat- | panies will share equally costs and | ||
| ing seasonal allergic | profits of further development; | |||
| rhinitis) | Sepracor retains rights to copro- | |||
| mote in U.S.; Janssen has rights | ||||
| elsewhere (2/98) | ||||
| Sequenom* | Bruker-Franzen | Collaborative agree- | ND | Bruker-Franzen will upgrade the |
| Analytik GmbH | ment to develop high- | hardware and software interfaces | ||
| (Germany) | speed mass spectrometer | of its instruments to enable them | ||
| dedicated to process | to process Sequenom's Spectro- | |||
| Sequenom's Spectro- | Chips exclusively (1/98) | |||
| Chips for DNA analysis | ||||
| (functional microarrays) | ||||
| Signal | DuPont Merck | Collaboration on drugs | $25M | 3-year collaboration; DuPont will |
| Pharmaceuticals | Pharmaceutical Co. | for hepatitis C and | (equity; | provide research funding, and up-front |
| Inc.* | (partnership between | HIV infection; use of | % ND) | and milestone payments; DuPont |
| the DuPont Co. | Signal's high-throughput | will buy equity stake in Signal's | ||
| [NYSE:DD] and | screening assays to | IPO; Signal will screen for and | ||
| Merck & Co. Inc. | identify virus-specific | identify leads; DuPont will opti- | ||
| [NYSE:MRK]) | gene-regulating targets | mize leads, and develop and mar- | ||
| ket products; Signal gets royalties | ||||
| (1/98) | ||||
| Nippon Kayaku | Collaboration to | ND | Nippon will provide research fund- | |
| Co. Ltd. (Japan) | develop Nippon's small | ing to Signal for 1st 2 years and | ||
| molecule nerve growth | will continue to conduct animal | |||
| factor mimetic as a drug | pharmacology studies; Signal will | |||
| for treating peripheral | optimize compound prior to clin- | |||
| neuropathies; use of | ical trials via combinatorial chem- | |||
| Signal's human neuronal | istry and neuronal cell lines; com- | |||
| cell lines to optimize | panies will co-develop product and | |||
| compound and character- | share marketing rights worldwide | |||
| ize its mode of action | except Japan (2/98) | |||
| Synaptic | Glaxo Wellcome | Licensing agreement | $2M | Synaptic had already licensed |
| Pharmaceutical | plc (NYSE:GLX; U.K.) | for certain of Synaptic's | these rights to Merck & Co. under | |
| Corp. | alpha adrenergic receptor | an 11/93 agreement; thus Merck | ||
| patents and functional- | had to approve the transaction | |||
| use patents for treating | with Glaxo; Glaxo gets non-exclu- | |||
| benign prostatic hyper- | sive license to receptor patents; | |||
| plasia | Synaptic got $2M up front and will | |||
| get additional payment if Merck | ||||
| exercises option on nonexclusive | ||||
| license to functional-use patents | ||||
| (option expires 5/22/99); Synaptic | ||||
| gets milestones under certain con- | ||||
| ditions and royalties (3/98) | ||||
| Grunethal GmbH | Cooperative agreement | ND | Grunethal will conduct preclinical | |
| (Germany) | to develop drugs for | and clinical studies; Synaptic | ||
| treating pain via | retains manufacturing and market- | |||
| Synaptic's cloned human | ing rights in U.S., Canada and | |||
| receptor-targeted drug | Mexico; Grunethal has those rights | |||
| design technology and | in Europe and Central and South | |||
| Grunethal's pain model | America; companies will share | |||
| systems; initial focus | rights elsewhere; companies are | |||
| on alpha-2 adrenergic | each responsible for own expenses | |||
| receptors | during research phase and will | |||
| share equally all costs through | ||||
| Phase II trials (1/98) | ||||
| Synt:em* | Laboratoires | Research collaboration | ND | Servier will develop and market |
| (France) | Servier (France) | on vectorization of anti- | products; Synt:em gets milestone | |
| cancer molecules using | payments; further details ND | |||
| Synt:em's Pep:trans | (2/98) | |||
| technology (enables | ||||
| creation of peptidic | ||||
| vectors able to cross | ||||
| cell membranes, thus | ||||
| internalizing drugs into | ||||
| cancer cells) | ||||
| Therion Biologics | Pasteur Merieux | Collaboration to | $25M | Cross-licensing agreement; Pasteur |
| Corp.* | Connaught | develop live recom- | (equity; | gets exclusive rights to certain of |
| (Canada; member | binant pox virus | % ND) | Therion's therapeutic cancer vac- | |
| of the Rhone- | vector-based thera- | cines; Therion gets access to cer- | ||
| Poulenc Group) | peutic vaccines for | tain of Pasteur's pox virus vector | ||
| and its affiliate | colorectal and lung | technologies; Pasteur gets exclu- | ||
| Virogenetics | cancer and melanoma | sive worldwide rights to Therion's | ||
| Corp.* | therapeutic melanoma vaccines | |||
| and carcinoembryonic antigen | ||||
| (CEA)-based therapeutic vaccines; | ||||
| Therion gets $25M in milestones; | ||||
| Pasteur made initial equity invest- | ||||
| ment in Therion (1/98) | ||||
| Transgene SA | Schering-Plough | Research collaboration | $88M | 5-year collaboration; Schering- |
| (France) | Corp. (NYSE:SGP) | and license agreement; | Plough gets rights to existing and | |
| use of Transgene's | future adenoviral gene technology | |||
| adenoviral gene delivery | for use with p53 gene; Schering- | |||
| systems with Schering- | Plough has option to license Trans- | |||
| Plough's p53 tumor | gene's adenoviral systems for up | |||
| suppressor gene (and | to 5 additional genes; Transgene | |||
| several other genes) to | gets $8M in initial license fees; if | |||
| develop gene therapy | Schering-Plough exercises options | |||
| products | for all 6 genes, Transgene gets | |||
| $88M (licensing fees, research | ||||
| funding, milestones); Transgene | ||||
| also gets royalties (2/98) | ||||
| Triangle | Bukwang Pharma- | Licensing of L-FMAU | $6M | Triangle licensed rights to product |
| Pharmaceuticals | ceuticals Ind. Co. | (a pyrimidine nucleo- | for all human antiviral applications | |
| Inc. | Ltd. (South Korea) | side analogue intended | worldwide except in Korea; Bukwang | |
| for treating hepatitis B | gets up-front fee of $6M, milestone | |||
| infection) | payments and royalties (2/98) | |||
| Vanguard Medica | Stiefel | R&D collaboration | $8M | Vanguard responsible for clinical |
| Group plc (U.K.) | Laboratories Inc.* | on VML 262 as a | development through Phase II, at | |
| topical treatment for | which point Stiefel will take over | |||
| psoriasis (compound was | clinical trials (which it will fund); | |||
| originally isolated from | Stiefel gets product rights in Euro- | |||
| marigolds and is now | pean Union and Latin America; | |||
| chemically synthesized; | Stiefel will reimburse some of | |||
| Phase II trials initiated | Vanguard's preclinical develop- | |||
| 2/98) | ment costs; Vanguard will get $8M | |||
| in milestones over 4-5 years, as | ||||
| well as royalties (3/98) | ||||
| Xenova Group plc | Eli Lilly and Co. | R&D collaboration on | $35M | Xenova and MetaXen will get |
| (U.K.) and its sub- | (NYSE:LLY) | small molecule inhib- | $35M in license fees, research | |
| sidiary, MetaXen LLC | itors of plasminogen | funding and milestones, as well as | ||
| activator inhibitor | royalties; Lilly gets exclusive | |||
| (PAI-1) from Xenova's | worldwide rights to PAI-1 inhibit- | |||
| natural products library | ors and related technology for use | |||
| as antithrombotic drugs | in cardiovascular medicine; Meta- | |||
| for chronic use | Xen will conduct preclinical work; | |||
| Lilly responsible for clinical trials | ||||
| and product registrations as well | ||||
| as marketing (2/98) | ||||
| NOTES: | ||||
| # This chart contains information on new agreements only, covering the time between 1/1/98 and 3/24/98. It does not include arrangements that are classified strictly as production, manufacturing, marketing and/or distribution and supply agreements; a chart covering these arrangements will appear in the 4/13/98 issue of BioWorld Financial Watch. | ||||
| A chart covering modified agreements and terminated agreements between big pharma and biotech companies for the same time period (1/1/98 3/24/98) also will appear in the 4/13/98 issue of BioWorld Financial Watch. | ||||
| ND = Not disclosed, reported and/or available; LSE = London Stock Exchange | ||||
| * Private companies are indicated with an asterisk. | ||||
| ** Unless otherwise noted, the trading symbols for public biotechnology companies can be found by referring to the BioWorld Stock Report For Public Biotechnology Companies on pp. 15-16. | ||||
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