| Biotech | Pharma Company | Type/Product Area | Amount | Terms/Details (Month) |
| Company** | (Symbol/Country) | |||
| (Country) | ||||
| I. MODIFIED AGREEMENTS | ||||
| Advanced Tissue | Smith & Nephew | Expansion of 4/96 | $111M | Companies signed binding letter |
| Sciences Inc. | plc (U.K.) | joint venture to com- | (equity; | of intent to expand joint venture; |
| mercialize Dermagraft | % ND) | Advanced Tissue gets $35M over | ||
| for treating diabetic | next 12 months for additional | |||
| foot ulcers to include | indications, including immediate | |||
| indications of venous | $20M in equity purchase, $16M | |||
| and pressure ulcers as | in milestones and 1-time payment | |||
| well as commercial- | of $10M for demonstrating ability | |||
| ization of Dermagraft- | of Dermagraft-TC for treating | |||
| TC for treating burns | pressure sores (1/98) | |||
| Allelix Biophar- | Eli Lilly Canada | Expansion of 1989 | ND | Expansion will increase Lilly's |
| maceuticals Inc. | Inc. (unit of Eli | basic research collab- | total investment in Allelix to | |
| (Canada) | Lilly and Co.; | oration to apply new | more than US$21M since partner- | |
| NYSE:LLY) | technologies to 2 drug | ship began; collaboration already | ||
| discovery programs | extended once in 1/95 (1/98) | |||
| (excitatory amino acid | ||||
| receptors as targets for | ||||
| drugs to treat central | ||||
| nervous system dis- | ||||
| orders; neuropeptide Y | ||||
| receptor as target for | ||||
| drugs to treat eating | ||||
| disorders) | ||||
| Alza Corp. | Janssen Pharma- | Expansion of agreement | $21.5M | Alza will make 1-time payment of |
| ceutica Inc. | to develop an E-Trans | $21.5M to Janssen and will share | ||
| (Belgium; unit of | fentanyl product for | operating profits from U.S. sales | ||
| Johnson & John- | treating acute pain | and get royalties on sales else- | ||
| son; NYSE:JNJ) | (currently in Phase III | where; Janssen has right to market | ||
| trials; uses electric cur- | product and Alza has right to co- | |||
| rent to control drug | promote in U.S. (1/98) | |||
| administration through | ||||
| skin) | ||||
| Aurora | Eli Lilly and Co. | Aurora provided | ND | Aurora and Lilly signed a collab- |
| Biosciences | (NYSE:LLY) | Lilly with a sublicense | oration in 1/97 giving Lilly | |
| Corp. and Sibia | to Sibia's transcription- | access to Aurora's technologies | ||
| Neurosciences | based functional bio- | for use in its internal drug discov- | ||
| Inc. | assay for drug screening, | ery program; Aurora and Sibia | ||
| to be used in conjunc- | cross-licensed each other's drug | |||
| tion with Aurora's fluor- | screening technologies in 1/97 and | |||
| escent assay technol- | Aurora has now granted Lilly a | |||
| ogies and other drug | sublicense; Sibia got up-front pay- | |||
| screening services | ment, annual maintenance fees and | |||
| royalties (1/98) | ||||
| Aurora | Merck & Co. Inc. | Aurora provided | ND | Aurora and Merck signed a collab- |
| Biosciences | (NYSE:MRK) | Merck with a sub- | oration in 12/97 giving Merck | |
| Corp. and Sibia | license to Sibia's | access to Aurora's technologies | ||
| Neurosciences | patent on high-through- | for use in its internal drug discov- | ||
| Inc. | put drug screening, for | ery program; Aurora and Sibia | ||
| use in conjunction | cross-licensed each other's drug | |||
| with Aurora's fluor- | screening technologies in 1/97 and | |||
| escent assay technol- | Aurora now has granted Merck a | |||
| ogies and other drug | sublicense; Sibia got up-front pay- | |||
| screening services | ment (1/98) | |||
| Connetics Corp. | Soltec Research | Connetics exercised its | ND | Connetics gets exclusive rights to |
| Pty Ltd. | option under 6/96 agree- | develop and market product in | ||
| (Australia) | ment to license clobeta- | North America (1/98) | ||
| sol mousse for treating | ||||
| severe dermatoses (high- | ||||
| potency corticosteroid | ||||
| formulated as quick- | ||||
| break foam) | ||||
| Corixa Corp. | Pasteur Merieux | Extension and expan- | ND | Relationship stems from prior |
| Connaught (unit | sion of 3/97 collabora- | option agreement for Pasteur Mer- | ||
| of Rhone-Poulenc | tion on use of Corixa's | ieux to license exclusive rights to | ||
| Group; France) | protein adjuvant LeIF | LeIF as adjuvant; now, Pasteur | ||
| (Leishmanial eukaryotic | Merieux has received new option | |||
| initiation factor) in | to commercialize LeIF in same | |||
| vaccines for infectious | disease areas as previously; this | |||
| diseases; expanded to | option expires 6/30/98 (1/98) | |||
| include comparisons of | ||||
| LeIF to other adjuvants | ||||
| SmithKline | Extension of Smith- | $2M | As part of 3/97 cancer vaccine | |
| Beecham Biologic- | Kline's option under | collaboration, Corixa granted | ||
| als SA (Belgium; | 3/97 cancer vaccine | SmithKline 2 options for licensing | ||
| unit of SmithKline | agreement to license | its programs for vaccine develop- | ||
| Beecham plc; | early-stage antigen | ment; SmithKline paid $2M to | ||
| NYSE:SBH; U.K.) | discovery program for an | extend the 1st option until 9/30/99 | ||
| undisclosed cancer target | (the 2nd option must be acted on | |||
| by 3Q:98) (2/98) | ||||
| Cytel Corp. | Nextran unit of | Expansion and exten- | ND | New agreement allows for broader |
| Baxter Healthcare | sion of 10/96 collab- | application of Cytel's carbohy- | ||
| Corp. (NYSE:BAX) | oration on Cytel's alpha | drate products (made via sugar | ||
| galactose carbohydrate | nucleotide cycling technology); | |||
| product for use in anti- | Cytel has exclusive agreement to | |||
| transplant rejection | supply products to Nextran; Cytel | |||
| device to include other | gets milestones; Baxter invested | |||
| carbohydrate products | $1M in Cytel's $8.4M private | |||
| for treating rejection | placement (12/97); Cytel will | |||
| associated with xeno- | develop and manufacture products | |||
| transplantation | (2/98) | |||
| Emisphere | Eli Lilly and Co. | Expansion of 2/97 | ND | Lilly executed 2 license agree- |
| Technologies | (NYSE:LLY) | agreement to use | ments and made 2 milestone pay- | |
| Inc. | Emisphere's technology | ments to Emisphere (both are part | ||
| for oral delivery of | of the terms of the original agree- | |||
| therapeutic proteins and | ment) (3/98) | |||
| exercise of 2 options to | ||||
| license technology for | ||||
| 2 specific Lilly proteins | ||||
| (1 in osteoporosis; 1 in | ||||
| endocrinology, including | ||||
| growth disorders) | ||||
| Epimmune Inc. | G.D. Searle & Co. | Definitive agreement | $100M | Letter of intent signed 9/97, at |
| (subsidiary of | (wholly owned sub- | to collaborate on cancer | (13.4% | which time Searle invested $5M |
| Cytel Inc.) | sidiary of Monsanto | vaccines developed via | equity) | in Cytel; in definitive agreement, |
| Co.; NYSE:MTC) | Epimmune's library of | Searle invested additional $3.9M | ||
| antigenic cancer epitopes | in Cytel preferred stock and $6.1M | |||
| and immunostimulant | in Epimmune preferred stock; | |||
| technology (PADRE) | Cytel simultaneously invested | |||
| $3.9M in Epimmune preferred | ||||
| stock; Searle now owns 13.4% of | ||||
| Epimmune, while Cytel owns the | ||||
| rest; preclinical and clinical mile- | ||||
| stones could total $100M over | ||||
| next 10-12 years; Searle gets world- | ||||
| wide exclusive rights to Epimmune's | ||||
| epitope and PADRE technologies | ||||
| in cancer field (excluding rights | ||||
| previously granted elsewhere); | ||||
| Epimmune gets royalties (3/98) | ||||
| Genome | Schering-Plough | Extension of 12/95 | $7M | Collaboration extended through |
| Therapeutics | Corp. (NYSE:SGP) | collaboration on anti- | 3/31/00; guaranteed payments to | |
| Corp. | infective agents for drug- | Genome Therapeutics raised from | ||
| resistant bacteria, includ- | $13M to $20M (it can also get as | |||
| ing Staphylococcus | much as $23.5M more in mile- | |||
| aureus, via Genome | stones) (3/98) | |||
| Therapeutics' genomics- | ||||
| based high-throughput | ||||
| screening, target vali- | ||||
| dation and assay | ||||
| development | ||||
| Human Genome | Takeda Chemical | Takeda exercised option | ND | Takeda exercised its option to |
| Sciences Inc. | Industries Ltd. | under 6/95 agreement | develop and commercialize pro- | |
| (Japan) | to license Human Ge- | duct in Japan; Human Genome | ||
| nome's genomics-derived | got option fee for these rights and | |||
| product candidate mye- | will get milestones and royalties; | |||
| loid progenitor inhibitory | further details ND (2/98) | |||
| factor-1 (currently in U.S. | ||||
| Phase I trials for protecting | ||||
| hematopoietic progenitor | ||||
| cells from effects of | ||||
| chemotherapy) | ||||
| Incyte | Novartis AG | Expansion of 6/97 | ND | Novartis gets nonexclusive access |
| Pharmaceuticals | (Switzerland) | database partnership | to LifeSeq database in exchange | |
| Inc. | to include Incyte's | for annual access fees; further | ||
| LifeSeq gene sequence | details ND (1/98) | |||
| and expression database | ||||
| Pfizer Inc. | Extension and expan- | ND | Pfizer will continue to have access | |
| (NYSE:PFE) | sion of 6/94 genomic | to Incyte's databases, including | ||
| database partnership to | its LifeSeq gene sequence and | |||
| include LifeSeq FL data- | expression database as well as | |||
| base of full-length genes | others; collaboration extended for | |||
| and LifeSeq GeneAlbum | 3 years (intent announced 12/97); | |||
| DNA clone set | financial details ND (2/98) | |||
| LeukoSite Inc. | Warner-Lambert | Extension of 11/96 | ND | Two-year extension of collabora- |
| Co. (NYSE:WLA) | collaboration on small | tion (already expanded once in | ||
| molecule antagonists to | 11/97) (1/98) | |||
| the CCR5 and CXCR4 | ||||
| receptors (chemokine | ||||
| coreceptors used by | ||||
| HIV to enter T cells) | ||||
| Ligand | Eli Lilly and Co. | Extension of Ligand's | $20M | Lilly extended Ligand's option so |
| Pharmaceuticals | (NYSE:LLY) | option (under 11/97 | that Ligand has additional time to | |
| Inc. | alliance on meta- | complete its evaluation and asses- | ||
| bolic diseases) to | ment of product; if Ligand exer- | |||
| acquire selected rights | cises option, Lilly gets milestones | |||
| to 1 of Lilly's specialty | of $20M in Ligand stock; if Ligand | |||
| drugs in certain mar- | does not exercise option, it can | |||
| kets of interest to | elect to sell $20M in equity to | |||
| Ligand | Lilly at 20% premium to market | |||
| (3/98) | ||||
| SmithKline | Expansion of 2/95 | ND | The collaboration was expanded | |
| Beecham plc | collaboration on small | twice; in 2/97, SmithKline exer- | ||
| (NYSE:SBH; U.K.) | molecule, orally available | cised its option to include a 3rd | ||
| drugs to control hemato- | drug discovery target and bought | |||
| poiesis; use of Ligand's | $2.5M in Ligand stock; in 8/97, | |||
| STAT technology (signal | SmithKline extended the term of | |||
| transducers and activators | the collaboration and bought a | |||
| of transcription) to target | $2.5M convertible note (although | |||
| hematopoietic growth | both these events occurred in 1997, | |||
| factors | Ligand announced them in 1998) | |||
| (3/98) | ||||
| MedImmune Inc. | SmithKline | Finalized agreement | $85M | Agreement, proposed 12/97, was |
| Beecham plc | (from 12/97) to develop | subject to clearance under anti- | ||
| (NYSE:SBH; U.K.) | human papillomavirus | trust laws, which occurred (1/98) | ||
| (HPV) vaccines for pre- | ||||
| venting cervical cancer | ||||
| and genital warts | ||||
| Onyx | Parke-Davis | Extension of 5/95 | $25M | Collaboration extended for 3 years; |
| Pharmaceuticals | (division of | collaboration on drugs | Onyx gets $25M in committed | |
| Inc. | Warner-Lambert Co.; | that affect cell-cycle | funding plus milestones; Warner- | |
| NYSE:WLA) | regulation; for treat- | Lambert also gets marketing rights | ||
| ing cancer and hyper- | in Japan (as well as rest of world); | |||
| proliferative diseases | Onyx gets milestones tied specifi- | |||
| cally to development efforts in | ||||
| Japan (1/98) | ||||
| OSI Pharma- | Wyeth-Ayerst | Exercise of option to | ND | Wyeth-Ayerst gets exclusive |
| ceuticals Inc. | Laboratories | license series of small | worldwide license to compounds; | |
| (division of Ameri- | molecule, gene-transcrip- | further details ND (1/98) | ||
| can Home Products | tion-based compounds | |||
| Corp.; NYSE:AHP) | that modulate expression | |||
| of phosphoenol pyruvate | ||||
| carboxykinase (PEPCK) for | ||||
| treating Type II diabetes | ||||
| Repligen Corp. | Glaxo Wellcome | Extension of 11/94 | ND | One-year extension; Glaxo will use |
| plc (NYSE:GLX; U.K.) | collaboration on chemo- | assay to screen its internal com- | ||
| kine inhibitors; com- | pound library; Repligen will | |||
| panies have jointly | supply Glaxo with 1 of its carbo- | |||
| developed high-through- | hydrate analogue combinatorial | |||
| put screening assay to | libraries for screening, too; Glaxo | |||
| identify small molecules | gets worldwide rights to any prod- | |||
| that block interaction of | ucts; Repligen gets research sup- | |||
| pro-inflammatory chemo- | port and royalties; Glaxo has | |||
| kine with its receptor | option to acquire rights to active | |||
| compounds from Repligen's | ||||
| library (1/98) | ||||
| Ribozyme | Parke-Davis | Definitive agreement | ND | Letter of intent signed 12/97; |
| Pharmaceuticals | (division of | on collaboration to | Ribozyme Pharmaceuticals will | |
| Inc. | Warner-Lambert Co.; | evaluate specific disease- | design and synthesize ribozymes | |
| NYSE:WLA) | related genes for drug | against target genes designated by | ||
| intervention using | Parke-Davis; financial terms ND | |||
| Ribozyme's target val- | (3/98) | |||
| idation technology | ||||
| (involves use of ribo- | ||||
| zymes to discover gene | ||||
| function and validate | ||||
| gene targets) | ||||
| Trega | Ono Pharmaceutical | Letter of intent to | ND | Ono will fund additional research |
| Biosciences Inc. | Co. Ltd. (Japan) | expand 6/97 collabor- | and pay milestones and royalties; | |
| ation on orally active | Trega will optimize and screen | |||
| small molecules for | lead compounds discovered by | |||
| treating diseases medi- | Ono in new area of interest; other | |||
| ated by melanocortin | details ND (2/98) | |||
| receptor (i.e., inflam- | ||||
| matory diseases) to | ||||
| include a new target of | ||||
| interest to Ono | ||||
| Vimrx | Baxter Healthcare | Official naming of new | $130M | Companies signed letter of intent |
| Pharmaceuticals | Corp. (subsidiary of | cell therapy company | (equity; | to form the new company (which |
| Inc. | Baxter International | Nexell Therapeutics | % ND) | is 80% owned by Vimrx and 20% |
| Inc.; NYSE:BAX) | Inc. (formed in 1997 | owned by Baxter) in 6/97; the | ||
| to develop cell therapies | definitive agreement was signed in | |||
| for cancer and other | 10/97 and Vimrx shareholders | |||
| diseases by combining | approved the deal in 12/97; Baxter | |||
| Baxter's ex vivo cellular | and Vimrx together contributed | |||
| selection and storage | $40M to fund Nexell; Baxter is | |||
| business with Vimrx's | responsible for manufacturing, | |||
| access to gene therapy | sales, marketing and distribution | |||
| and genomics technology) | of products; Nexell will focus on | |||
| R&D, partnerships and marketing | ||||
| development (2/98) | ||||
| II. TERMINATED AGREEMENTS | ||||
| Amylin | Johnson & Johnson | Termination of 6/95 | — | Johnson & Johnson provided 6 |
| Pharmaceuticals | (NYSE:JNJ) | collaboration on Pram- | months' notice of its intent to | |
| Inc. | lintide (synthetic ana- | terminate the collaboration, saying | ||
| logue of human hormone | it was no longer in its best inter- | |||
| amylin) for treating | ests; all product rights return to | |||
| Types I and II diabetes | Amylin, which will restructure its | |||
| (currently in Phase III | operations and reduce workforce | |||
| trials) | by 25% so it can continue product | |||
| development (3/98) | ||||
| Anergen Inc. | Novo Nordisk A/S | Termination of 8/93 | — | This collaboration was extended |
| (NYSE:NVO; | collaboration on use of | for 2 years in 4/96, but Novo has | ||
| Denmark) | AnergiX technology | now terminated it, as part of its | ||
| (inactivates disease- | change in strategic direction; all | |||
| related T cells) for | product rights return to Anergen; | |||
| various diseases, includ- | Novo will reimburse Anergen for | |||
| ing multiple sclerosis | cost of ongoing clinical trial; Aner- | |||
| (Phase I trial ongoing) | gen has no future obligations to | |||
| Novo; Anergen will restructure its | ||||
| operations and reduce workforce | ||||
| (2/98) | ||||
| Immusol Inc.* | Pfizer Inc. | Conclusion of 3/95 | — | Partnership will not be renewed; |
| (NYSE:PFE) | collaboration to | Pfizer will fund program through | ||
| develop ribozyme gene | 5/98, after which Immusol will | |||
| therapy for treating | continue product development | |||
| HIV infection (program | (HIV gene therapy currently in | |||
| was part of Pfizer's | Phase I trials) (3/98) | |||
| R&D initiative | ||||
| Pfizergen) | ||||
| NaPro | Baker Norton | Termination of 1993 | $14.5M | Partners terminated their agree- |
| BioTherapeutics | Pharmaceuticals | development and | ment after the FDA ruled in 12/97 | |
| Inc. | Inc. (wholly owned | marketing agreement | that Ivax's paclitaxel-based drug | |
| subsidiary of Ivax | on paclitaxel (compound | Paxene for treating AIDS-related | ||
| Corp.; AMEX:IVX) | extracted from needles | Kaposi's sarcoma might not get | ||
| and limb stock of | marketing approval until 8/04; | |||
| ornamental yew trees) | Ivax gets royalty-free, nonexclu- | |||
| sive license to NaPro's pending | ||||
| patents on stable formulation of | ||||
| paclitaxel in U.S., Europe and cer- | ||||
| tain other markets; NaPro gets | ||||
| $6M cash, $6.4M on issuance of | ||||
| patents and the return of 1.1M | ||||
| shares of its stock ($2.1M) held by | ||||
| Ivax; NaPro will supply a certain | ||||
| amount of paclitaxel to Ivax (3/98) | ||||
| NOTES: | ||||
| # This chart contains information on modified and terminated agreements only, covering the time period between 1/1/98 and 3/24/98. It does not include arrangements that are classed strictly as production, marketing and/or distribution agreements, nor does it include any collaborations that involve agricultural product development. | ||||
| For a chart listing new collaborations between big pharma and biotech companies for the same time period (1/1/98 - 3/24/98), see the 3/30/98 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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