| Biotech | Pharma | Type/Product Area | Amount | Terms/Details (Month) |
| Company** | Company | |||
| (Country) | (Symbol/ | |||
| Country) | ||||
| Affymetrix Inc. | Beckman Coulter | Series of agreements | ND | Companies will cooperate in devel- |
| Inc. (NYSE:BEC) | to commercialize DNA | oping and commercializing DNA | ||
| probe arrays (including | arrays and related instrumentation | |||
| GeneChip) under patents | for research and diagnostics mar- | |||
| owned by, or licensed to, | kets; companies may provide | |||
| the 2 parties | access to 3rd parties (8/98) | |||
| Eli Lilly and Co. | EasyAccess agreement; | ND | 3-year agreement; Lilly gets | |
| (NYSE:LLY) | GeneChip arrays, instru- | broad access to technology for use | ||
| mentation and software | in its R&D programs; Lilly gets | |||
| for monitoring of gene | volume discount (9/98) | |||
| expression | ||||
| Agouron | Japan Energy | License agreement on | $26M | Agouron gets exclusive rights to |
| Pharmaceuticals | Corp. (Japan) | Japan Energy's HIV | develop and commercialize drug | |
| Inc. | protease inhibitor | in North America, Europe and | ||
| JE-2147 (especially | elsewhere; Japan Energy retains | |||
| for treating drug- | rights in Japan, Korea and Taiwan; | |||
| resistant HIV) | Japan Energy gets $26M in fees, | |||
| including $6M initial license fee, | ||||
| plus royalties (6/98) | ||||
| Shionogi & Co. | License agreement on | $40M | Agouron gets exclusive rights to | |
| Ltd. (Japan) | Shionogi's 2nd-gener- | develop and commercialize drug | ||
| ation non-nucleoside | in North America, Europe and | |||
| HIV reverse transcrip- | elsewhere; Shionogi retains rights | |||
| tase inhibitor S-1153 | in Japan, Korea and Taiwan; Shi- | |||
| (especially for treating | onogi gets $40M in fees, including | |||
| drug-resistant HIV) | $10M initial license fee, plus | |||
| royalties (6/98) | ||||
| Aphton Corp. | SmithKline | Collaboration and | $15M | Companies will conduct clinical |
| Beecham Biologi- | license agreement on | (equity; | trials jointly; SmithKline will fund | |
| cals SA (Belgium; | Aphton's Gonad- | % ND) | all costs of product development | |
| unit of SmithKline | immune anti-gonado- | and approvals; SmithKline gets | ||
| Beecham plc; | tropin releasing hormone | exclusive worldwide rights to | ||
| NYSE:SBH; U.K.) | (anti-GnRH) synthetic | Aphton's patents and technology; | ||
| peptide vaccines for | Aphton gets royalties but no up- | |||
| diagnosis, treatment and | front or milestone payments; | |||
| prevention of GnRH- | SmithKline bought $5M in equity | |||
| related cancers and other | (0.24M shares at premium to mar- | |||
| diseases | ket); Aphton has 2-year option to | |||
| sell another $5M in equity to | ||||
| SmithKline; if option is exercised, | ||||
| SmithKline has 90 days to buy an | ||||
| additional $5M in equity (6/98) | ||||
| Aviron | Becton Dickinson | Supply agreement; use | ND | Worldwide multiyear supply |
| and Co. (NYSE: | of Becton Dickinson's | agreement; terms ND (8/98) | ||
| BDX) | AccuSpray noninvasive | |||
| nasal spray delivery | ||||
| system for administration | ||||
| of Aviron's FluMist intra- | ||||
| nasal influenza vaccine | ||||
| Axys | Parke-Davis (divi- | Combinatorial chemistry | $20M | 3-year agreement; Parke-Davis |
| Pharmaceuticals | sion of Warner- | agreement based on Axys' | gets library plus enabling technol- | |
| Inc. | Lambert Co.; | generic compound screen- | ogies and synthetic protocols for | |
| NYSE:WLA) | ing library (consists of | recreating the library and making | ||
| multiple small-molecule | others; Axys gets payments of | |||
| synthetic organic compound | $20M; further details ND (6/98) | |||
| libraries) | ||||
| Wyeth-Ayerst | Pharmacogenomics | ND | Wyeth-Ayerst will conduct clini- | |
| Laboratories (divi- | agreement; clinical | cal study on Axys' gene variant; | ||
| sion of American | study of role played by | Axys will provide patient geno- | ||
| Home Products | polymorphism in cyto- | typing and intellectual property; | ||
| Corp.; NYSE:AHP) | chrome p450 3A4 gene | further details ND (7/98) | ||
| in metabolism of 2 classes | ||||
| of marketed drugs | ||||
| BioCryst | The R.W. Johnson | Collaboration and | $55M | BioCryst gets $6M up front and |
| Pharmaceuticals | Pharmaceutical | license agreement on | (equity; | a $6M equity investment from |
| Inc. | Research Institute | BioCryst's orally | % ND) | Johnson & Johnson Development |
| and Ortho-McNeil | active influenza neura- | Corp.; BioCryst also gets mile- | ||
| Pharmaceuticals | minidase inhibitors for | stones and royalties; R.W. Johnson | ||
| Inc. (both Johnson & | treating and preventing | and Ortho get exclusive worldwide | ||
| Johnson companies; | viral influenza | rights to products (9/98) | ||
| NYSE:JNJ) | ||||
| Bioject Medical | Merck & Co. Inc. | Use of Bioject's needle- | ND | ND (7/98) |
| Technologies Inc. | (NYSE:MRK) | free jet injection sys- | ||
| tem to deliver selected | ||||
| Merck vaccines | ||||
| Cellegy | 3M Drug Delivery | Research agreement | ND | ND (6/98) |
| Pharmaceuticals | Systems | to evaluate combining | ||
| Inc. | Cellegy's Celledirm | |||
| inflammatory response | ||||
| modulator technology | ||||
| with 3M's Latitude | ||||
| transdermal drug | ||||
| delivery system | ||||
| Cellomics Inc.* | Merck & Co. Inc. | Agreement to develop | ND | ND (6/98) |
| (NYSE:MRK) | cell-based, high-content | |||
| screening platform (uses | ||||
| fluorescence-based | ||||
| assays) | ||||
| Cellomics Inc.* | Warner-Lambert | Agreement to develop | ND | ND (8/98) |
| Co. (NYSE:WLA) | fluorescence-based | |||
| cytotoxicity assays | ||||
| Cerebrus Holdings | Eli Lilly and Co. | Joint development of | ND | Cerebrus licensed the compound |
| plc (U.K.) | (NYSE:LLY) | Lilly's drug CEB-1555 | and will conduct clinical trials | |
| (selective 5HT1A | through Phase II; Lilly then has | |||
| receptor agonist) for | option of completing clinical devel- | |||
| treating delayed and | opment alone or in collaboration | |||
| anticipatory emesis | with Cerebrus; if it doesn't exer- | |||
| associated with cancer | cise option, Cerebrus can develop | |||
| chemotherapy | with or without new partner (9/98) | |||
| Cistron | Pasteur Merieux | Letter of intent to fund | $31M | Pasteur Merieux has 3-year option |
| Biotechnology Inc. | Connaught (unit | interleukin-1 beta (IL-1b) | (equity; | on exclusive license to use IL-1b |
| (OTC Bulletin Board: | of Rhone-Poulenc | vaccine adjuvant devel- | % ND) | as adjuvant for preventive and |
| CIST) | Group; NYSE:RP; | opment program | therapeutic vaccines; Cistron gets | |
| France) | $0.9M for preclinical research | |||
| during option period and $29M in | ||||
| milestones if Pasteur Merieux | ||||
| exercises option; Pasteur Merieux | ||||
| will buy $0.975M in Cistron | ||||
| stock (1.3M shares at $0.75/share) | ||||
| and a 3-year warrant to buy more | ||||
| shares (7/98) | ||||
| Cytoclonal | Bristol-Myers | License and research | $50M | Cytoclonal could get $50M in |
| Pharmaceutics Inc. | Squibb Co. | agreement; use of | research and support fees and | |
| (NYSE:BMY) | microbial fermentation | milestones, as well as royalties | ||
| to produce paclitaxel | (6/98) | |||
| and/or other taxanes; | ||||
| also, use of specific | ||||
| genes to enhance pro- | ||||
| duction | ||||
| Desmos Inc.* | Guidant Corp. | Collaboration to test | ND | Guidant will provide financial |
| (NYSE:GDT) | feasibility of improving | support; further details ND (7/98) | ||
| stent biocompatibility | ||||
| by coating them with | ||||
| Desmos' bioenhancing | ||||
| materials | ||||
| Epix Medical Inc. | Pfizer Inc. | Collaboration on use | ND | ND (9/98) |
| and Mallinckrodt | (NYSE:PFE) | of AngioMark enhanced | ||
| Inc. (NYSE:MKG) | magnetic resonance | |||
| imaging in diagnosis | ||||
| and monitoring of | ||||
| female sexual arousal | ||||
| dysfunction | ||||
| Gene Logic Inc. | Wyeth-Ayerst | Pharmacogenomics | ND | During 1st year of agreement, com- |
| Laboratories | alliance; use of Gene | panies will share costs of selecting | ||
| (division of Ameri- | Logic's gene expression | compounds and tissue samples to | ||
| can Home Products | technology to develop | be analyzed; Wyeth-Ayerst also | ||
| Corp.; NYSE:AHP) | database of gene expres- | gets access to flow-through chip | ||
| sion profiles to predict | technology; Gene Logic may non- | |||
| preclinical toxicity of | exclusively license products | |||
| Wyeth-Ayerst compounds | developed to 3rd parties (6/98) | |||
| Genomica Corp.* | Glaxo Wellcome | License agreement; use | ND | ND (7/98) |
| plc (NYSE:GLX; | of Genomica's bio- | |||
| U.K.) | informatics gene-dis- | |||
| covery software system | ||||
| for gene discovery and | ||||
| functional analysis | ||||
| Genset SA | Wyeth-Lederle | License agreement; use | $15M | Wyeth-Lederle gets exclusive |
| (France) | Vaccines (unit of | of Genset's genomic | worldwide rights to patent appli- | |
| American Home | data on Chlamydia | cations covering entire L2 genomic | ||
| Products Corp.; | pneumoniae and | sequences of both organisms for | ||
| NYSE:AHP) | C. trachomatis for | use in vaccines; Genset gets $15M | ||
| vaccines | initial license fee and milestones, | |||
| as well as royalties; Genset retain- | ||||
| ed rights for diagnostic, small | ||||
| molecule, therapeutic protein, gene | ||||
| therapy and cell therapy applica- | ||||
| tions of genomic data (8/98) | ||||
| Genzyme | Bayer Corp. | Genomics collaboration; | ND | Service agreement; Genzyme |
| Molecular | (unit of Bayer AG; | use of Genzyme Molec- | Molecular will provide gene expres- | |
| Oncology (division | Germany) | ular's SAGE technology | sion analysis for Bayer's drug can- | |
| of Genzyme Corp.) | (serial analysis of gene | didates (8/98) | ||
| expression) to identify | ||||
| genes for development | ||||
| of future drug candidates | ||||
| Igen International | Medinnova SF | License agreement; | ND | Igen acquired exclusive worldwide |
| Inc. | (Norway) | use of Medinnova's | rights to marker, which it will use | |
| cardiac marker (N- | in an Origen-based test (7/98) | |||
| terminal pro-atrial | ||||
| naturietic peptide) | ||||
| for detecting and | ||||
| monitoring cardiac- | ||||
| related diseases | ||||
| Ilex Oncology Inc. | Symphar SA | Joint development | ND | Ilex will conduct all clinical devel- |
| (Switzerland) | agreement on Symphar's | opment; Ilex can negotiate for all | ||
| orally active, apoptosis- | future rights to SR-45023A; fur- | |||
| inducing compound | ther details ND (9/98) | |||
| SR-45023A (bisphos- | ||||
| phonate ester deriv- | ||||
| ative that stimulates | ||||
| nuclear receptor FXR) | ||||
| for treating cancer | ||||
| ImmuLogic | Heska Corp. | License agreement; | ND | Heska gets exclusive worldwide |
| Pharmaceutical | (NASDAQ:HSKA) | use of ImmuLogic's | license to technology (except in | |
| Corp. | recombinant allergen | Japan, where rights are nonexclu- | ||
| technology for diag- | sive); ImmuLogic gets license fees, | |||
| nosis, immunotherapy | milestones and royalties (6/98) | |||
| and gene therapy appli- | ||||
| cations in humans and | ||||
| companion animals | ||||
| The Immune | Schering-Plough | Research collaboration | $80M | In preclinical stage of agreement |
| Response Corp. | Corp. (NYSE:SGP) | and option agreement | (1 year), Immune Response gets | |
| to combine Immune | $5M in initial fees, reimbursement | |||
| Response's GeneDrug | and milestones related to delivery | |||
| gene delivery technology | of IFN alfa-2b gene; if Schering | |||
| with Schering's interferon | exercises option to use delivery | |||
| (IFN) alfa-2b gene (among | system for additional genes, it will | |||
| others) as gene therapy prod- | pay $75M in licensing fees and | |||
| ucts for treating hepatitis | milestones; Immune Response also | |||
| B and C virus infection | gets royalties (7/98) | |||
| Immunex Corp. | SmithKline | License agreement; use | ND | SmithKline gets nonexclusive |
| Beecham plc | of Immunex's granulo- | license to protein; Immunex gets | ||
| (NYSE:SBH; U.K.) | cyte-colony stimulating | up-front fee, milestones and roy- | ||
| factor receptor in Smith- | alties (8/98) | |||
| Kline's R&D program (to | ||||
| screen and develop small- | ||||
| molecule compounds) | ||||
| Inspire | Kissei Pharma- | Strategic collaboration; | $17.5M | Inspire gets $17.5M in up-front |
| Pharmaceuticals | ceutical Co. Ltd. | development of Inspire's | (equity; | fee, equity investment and mile- |
| Inc.* | (Japan) | inhaled respiratory | % ND) | stones; Inspire also gets R&D |
| therapeutic INS 365 | funds and royalties; Kissei gets | |||
| (activates P2Y2 receptor | exclusive rights in Japan plus | |||
| to stimulate mucociliary | access to 2nd-generation ana- | |||
| clearance) for treating | logues of INS 365 for respiratory | |||
| chronic obstructive | uses (9/98) | |||
| pulmonary diseases | ||||
| Intercardia Inc. | Opocrin SpA | License agreement; use | >$1M | Intercardia gets exclusive world- |
| (Italy) | of Opocrin's OP2000 | wide license except in Japan and | ||
| (oligosaccharide derived | South Korea; Intercardia will con- | |||
| from heparin) for treat- | duct clinical trials; Opocrin gets | |||
| ing inflammatory | $1M in license fees as well as mile- | |||
| bowel disease | stones (7/98) | |||
| Irori Inc.* | Rhone-Poulenc | Combinatorial chemis- | $10.5M | 2-year collaboration; Irori gets |
| Rorer Inc. (sub- | try collaboration; devel- | (equity; | $0.8M on signing; Rhone-Poulenc | |
| sidiary of Rhone- | opment of ultra-high- | % ND) | will buy $4.5M in Irori equity and | |
| Poulenc Group; | throughput combina- | will pay licensing fee and mile- | ||
| NYSE:RP; France) | torial chemistry system | stones; Rhone-Poulenc has option | ||
| using Irori's Nano- | to buy an additional NanoReactor | |||
| Reactor technology | system (6/98) | |||
| (miniaturized micro- | ||||
| reactors for screening | ||||
| very large numbers of | ||||
| single compounds) | ||||
| Lexicon Genetics | DuPont Pharma- | Mouse functional gen- | ND | DuPont will subscribe to Lexicon's |
| Inc.* | ceuticals Inc. | omics agreements in- | OmniBank database and also gets | |
| volving Lexicon's Omni- | nonexclusive license to Lexicon's | |||
| Bank gene sequence data- | positive-negative selection and | |||
| base of mutant mouse | isogenic DNA patent portfolio; | |||
| clones and DuPont's | Lexicon gets license to DuPont's | |||
| Cre-lox technology | Cre-lox technology and certain | |||
| (creates tissue-specific | sublicensing rights; Lexicon gets | |||
| gene knockouts) | exclusive rights to use Cre-lox to | |||
| practice gene trapping in mouse | ||||
| embryonic cells; companies will | ||||
| pay each other royalties (8/98) | ||||
| LJL BioSystems | SmithKline | Advanced technology | ND | SmithKline gets early access to |
| Inc. | Beecham plc | access program for | LJL's advanced technologies | |
| (NYSE:SBH; U.K.) | LJL's high-throughput | (9/98) | ||
| screening systems, | ||||
| especially FLARe | ||||
| platform (fluorescence- | ||||
| based assays) | ||||
| MacroChem Corp. | American Home | License agreement; use | ND | MacroChem gets license fees, |
| Products Corp. | of MacroChem's SEPA | (includes | milestones and royalties; American | |
| (NYSE:AHP) | absorption enhancer for | equity) | Home will buy undisclosed | |
| transdermal drug delivery | amount of MacroChem common | |||
| of an American Home | stock; American Home will | |||
| Products drug (undisclosed) | develop and market product (7/98) | |||
| Medarex Inc. | Medac GmbH | Research collaboration | ND | ND (9/98) |
| (Germany) | and license agreement; | |||
| use of Medarex's HuMAb- | ||||
| mouse technology to make | ||||
| fully human monoclonal | ||||
| antibodies to Medac's | ||||
| CD30 cancer antigen | ||||
| (for treating Hodgkin's | ||||
| lymphoma) | ||||
| Molecular | Beckman Coulter | Collaboration to develop | ND | ND (9/98) |
| Dynamics Inc. | Inc. (NYSE:BEC) | robotic system to inte- | ||
| grate and automate | ||||
| operation of multiple | ||||
| MegaBACE 1000 DNA | ||||
| sequencing units | ||||
| Molecumetics Ltd. | Bristol-Myers | Research collaboration; | $45M | 3-year agreement; Bristol-Myers |
| (subsidiary of | Squibb Co. | screening of Molecu- | will screen 150,000 MolecuSet | |
| Tredegar Indus- | (NYSE:BMY) | metics' MolecuSet com- | compounds against a number of | |
| tries; NYSE:TG) | pounds for therapeutics | disease targets; Molecumetics gets | ||
| for inflammatory and | research funding and milestones of | |||
| immunological diseases; | $45M over 3 years; both firms will | |||
| initial focus on small- | work to optimize lead compounds; | |||
| molecule transcription | Molecumetics gets royalties (9/98) | |||
| factor inhibitors | ||||
| MorphoSys AG* | DuPont Pharma- | Collaboration and | ND | DuPont gets license to antibody |
| (Germany) | ceuticals Co. | licensing agreement; | library and has option to develop | |
| use of MorphoSys' | specific antibodies as therapeutics, | |||
| human combinatorial | in vitro or in vivo diagnostics or | |||
| antibody library to | components of high-throughput | |||
| generate antibodies for | screens; MorphoSys gets fees, | |||
| DuPont's drug discovery | milestones and royalties (8/98) | |||
| program | ||||
| NanoSystems | Merck & Co. Inc. | License agreement; use | $30M | NanoSystems gets $30M in pre- |
| LLC* | (NYSE:MRK) | of NanoCrystal tech- | commercialization payments as | |
| nology (to deliver | well as royalties (this is 3rd col- | |||
| poorly water-soluble | laboration between the companies) | |||
| drugs) to deliver an | (8/98) | |||
| undisclosed Merck drug | ||||
| NeuroSearch A/S | Pharmacia & | License agreement on | ND | Pharmacia & Upjohn acquired |
| (Denmark) and | Upjohn Inc. | anti-anxiety compound | worldwide rights except in Nor- | |
| Meiji Seika Kaisha | (NYSE:PNU; U.K.) | NS 2710 (gamma amino | dic markets, Japan and Asia, where | |
| (Japan) | butyric acid modulator; | NeuroSearch and Meiji retain | ||
| now in Phase II trials) | rights, respectively; Pharmacia & | |||
| Upjohn will make initial payment | ||||
| to companies as well as pay mile- | ||||
| stones and royalties (7/98) | ||||
| Pangea Systems | Eli Lilly and Co. | License agreement; | ND | ND (7/98) |
| Inc.* | (NYSE:LLY) | use of Pangea's bio- | ||
| informatics software in | ||||
| Lilly's genomics and | ||||
| target validation programs | ||||
| Hoechst-Ariad | License agreement on | ND | ND (8/98) | |
| Genomics Center | Pangea's computational | |||
| (joint venture | algorithms for cluster- | |||
| between Ariad | ing and alignment of | |||
| Pharmaceuticals | expressed sequence tags | |||
| Inc. and Hoechst | within large databases | |||
| Marion Roussel Inc.) | ||||
| Phytera Inc.* | Eli Lilly and Co. | Research collaboration; | ND | Lilly will provide compounds for |
| (NYSE:LLY) | use of Phytera's anti- | (includes | screening in Phytera's systems; | |
| fungal screens (genomics- | equity) | Lilly responsible for profiling, | ||
| based) plus its natural | lead optimization, development | |||
| product extracts (plant | and commercialization; Phytera | |||
| cell cultures and marine | gets up-front equity investment, | |||
| microbial libraries) to | research funds, milestones and | |||
| discover products for | royalties; Lilly gets worldwide | |||
| diagnosis, treatment and | rights to products (7/98) | |||
| prevention of infectious | ||||
| fungal diseases in humans | ||||
| and animals | ||||
| Phytopharm plc | Pfizer Inc. | Collaboration to develop | $39M | Pfizer will contribute $7M to |
| (U.K.) | (NYSE:PFE) | appetite suppressant | Phase I trial (about to begin) and | |
| based on P57 (product | $32M in license fees and mile- | |||
| derived from extract of | stones; Pfizer gets exclusive | |||
| South African plant) | worldwide license to drug (8/98) | |||
| Proteomix Inc. | Bayer Corp. (unit | Research collaboration | $3M | Bayer gets access to genes and will |
| (subsidiary of | of Bayer AG; | on series of osteoclast | pay $3M in milestones; further | |
| NovaDx Inter- | Germany) | genes as drug targets | details ND (9/98) | |
| national Inc.; VSE: | for metabolic bone | |||
| NVN; Canada) | disease | |||
| Orincon Tech- | Option on license to | ND | ND (7/98) | |
| nologies Inc. | Orincon's 2D electro- | |||
| phoresis image analysis | ||||
| software for use in | ||||
| proteomics research | ||||
| RiboGene Inc. | Roberts Pharma- | Option and license | $27M | Roberts bought $10M in equity |
| ceutical Corp. | agreement on Ribo- | (equity; | (1.4M shares of Series A non- | |
| (AMEX:RPC) | Gene's Emitasol | %ND) | voting convertible preferred stock | |
| (metoclopramide; | at $7/share); Roberts will conduct | |||
| intranasal drug for | all product development; after FDA | |||
| treating delayed-onset | approval, Roberts has 90-day exclu- | |||
| nausea and vomiting | sive option to license marketing rights | |||
| in cancer chemotherapy | in North America; if it exercises option, | |||
| patients) | RiboGene gets $10M; RiboGene also | |||
| gets royalties; RiboGene will provide | ||||
| $7M in development funds through | ||||
| submission of NDA (7/98) | ||||
| Ribozyme | Glaxo Wellcome plc | Genetic target valida- | ND | Glaxo will designate target genes |
| Pharmaceuticals | (NYSE:GLX; U.K.) | tion and discovery | and Ribozyme will design, synthe- | |
| Inc. | agreement via Ribo- | size and deliver GeneBloc rea- | ||
| zyme's technology and | gents; financial terms ND (7/98) | |||
| GeneBloc molecules | ||||
| (inhibit gene expression) | ||||
| Sepracor Inc. | Janssen Pharma- | License agreement on | ND | Janssen gets exclusive license to |
| ceutica NV | (+) norcisapride (isomer | all of Sepracor's worldwide rights | ||
| (Belgium; unit of | of active metabolite of | to norcisapride enantiomers; | ||
| Johnson & Johnson; | Janssen's marketed drug | Sepracor has option to co-promote | ||
| NYSE:JNJ) | Propulsid for treating | product in pediatric market (7/98) | ||
| heartburn due to gastro- | ||||
| esophageal reflux) | ||||
| Sugen Inc. | Taiho Pharma- | Alliance to develop | $70M | Taiho will help fund product devel- |
| ceutical Ltd. (Japan) | Sugen's angiogenesis | opment; Taiho gets marketing | ||
| inhibitors (including | rights in Japan; Sugen retains rights | |||
| SU5416, currently in | in rest of world; Sugen gets up-front | |||
| Phase I/II trials) for | payments, research funds and mile- | |||
| preventing and treating | stones totaling $70M; Sugen will | |||
| cancer | manufacture and supply product to | |||
| Taiho for sale in Japan (7/98) | ||||
| Tularik Inc.* | Japan Tobacco Inc. | Research collaboration; | ND | 3-year agreement; companies will |
| (Japan) | development of small- | share development and commer- | ||
| molecule therapeutics to | cialization costs and profits world- | |||
| regulate orphan nuclear | wide; Tularik gets exclusive rights | |||
| receptors (which are | in U.S. and Canada; Japan Tobacco | |||
| transcription regulators) | gets exclusive rights in Japan | |||
| and Korea (9/98) | ||||
| UroGen Corp. | Baxter Healthcare | Joint collaboration on | $25M | UroGen bought exclusive rights |
| (OTC Bulletin | Corp. (subsidiary of | gene therapies for | (>19% | to Baxter's gene transfer technol- |
| Board:UROG) | Baxter International | blood disorders; use of | equity) | ogy with 5,444 shares of Series A |
| Inc.; NYSE:BAX) | Baxter's recombinant | convertible preferred stock; Uro- | ||
| adenoviral vectors for | Gen may also buy rights to other | |||
| gene transfer and Uro- | gene therapy technologies by | |||
| Gen's tumor sensitization | paying 1.76M shares of common | |||
| and related technologies | stock and 324 shares of Series A | |||
| convertible preferred stock; Baxter | ||||
| will pay $22M-$25M to fund joint | ||||
| development of gene therapies and | ||||
| gets worldwide marketing rights (7/98) | ||||
| Vertex | Schering AG | Strategic alliance on | $88M | 5-year agreement; companies will |
| Pharmaceuticals | (Germany) | development of orally | co-manage R&D; Schering will | |
| Inc. | active neurophilin com- | provide $28M in up-front and | ||
| pounds to promote | research support over 5 years, plus | |||
| neural regeneration in | $60M in milestones; Vertex re- | |||
| treating neurological | tains manufacturing rights in | |||
| diseases | North America, where companies | |||
| will share marketing expenses and | ||||
| profits; Schering has right to man- | ||||
| ufacture products in Europe, the | ||||
| Middle East and Africa, where | ||||
| Vertex gets royalties; Vertex has | ||||
| option to manufacture bulk drug | ||||
| substance for other markets (8/98) | ||||
| Xenogen Corp.* | F. Hoffmann- | License agreement; eval- | ND | Roche will evaluate technology in |
| La Roche Ltd. | uation of Xenogen's biopho- | its preclinical drug development | ||
| (Switzerland) | tonic imaging technology | program; further details ND (9/98) | ||
| and up to 4 strains of | ||||
| bacteria genetically engi- | ||||
| neered with reporter | ||||
| genes that code for | ||||
| light-emitting proteins | ||||
| NOTES: | ||||
| # This chart contains information on new agreements only, covering the time between 6/16/98 and 9/21/98. 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 10/12/98 issue of BioWorld Financial Watch. The chart above also does not include any collaborations that involve agricultural product development (which are covered periodically in this publication). | ||||
| A chart covering modified agreements and terminated agreements between big pharma and biotech companies for the same time period (6/16/98 - 9/21/98) will also appear in the 10/12/98 issue of BioWorld Financial Watch. | ||||
| ND = Not disclosed, reported and/or available | ||||
| * 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. 13-14. | ||||
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