| Biotech Company** (Country) | Pharma Company (Symbol/Country) | Type/Product Area | Amount | Terms/Details (Month) |
| I. MODIFIED AGREEMENTS | ||||
| Abgenix Inc. | Pfizer Inc. (NYSE:PFE) | Expansion of 12/97 collaboration and license agreement on use of Abgenix'sXenoMouse technology to make fully human antibodies to 3 of Pfizer's antigentargets | $10M | Pfizer exercised option for 2nd antigen target (undisclosed; 1st targetis for oncology applications); with exercise of option, Abgenix gets $10Min cash plus royalties (10/98) |
| Allelix Biopharmaceuticals Inc. (Canada) | Eli Lilly and Co. (NYSE:LLY) | Extension and expansion of partnership dating from 1989 on productsfor treating psychiatric, neurological and eating disorders | ND | Glutamate receptor program (for psychiatric and neurological disorders)has been extended for 2 years; genetic target program (for eating disorders)has been extended for 1 year (12/98) |
| ArQule Inc. | Roche Bioscience (division of Roche Holding Ltd.; Switzerland) | Amendment to 9/96 collaboration on new therapeutics via ArQule's directedarrays (custom libraries of compounds closely analogous to leads providedby Roche Bioscience) | ND | Companies will continue collaboration in a different form (not defined)through 3/99; ArQule will provide Roche with screening libraries whilecontinuing to optimize a number of Roche compounds (10/98) |
| Axys Pharmaceuticals Inc. | Merck & Co. Inc. (NYSE:MRK) | Extension of 11/96 collaboration on small molecule inhibitors of cathepsinK (cysteine protease) as therapies for osteoporosis | ND | Original agreement signed with Arris Pharmaceutical Corp. (which mergedwith Sequana Therapeutics Inc. in 1/98 to form Axys); companies extendedcollaboration to 11/99; further details ND (12/98) |
| Corixa Corp. | SmithKline Beecham | Major expansion of 10/95 | $200M | Expanded agreement adds 5 new vaccine |
| Biologicals SA | collaboration on T cell- | (equity; | programs; SmithKline also has option to | |
| (Belgium; unit of | active vaccines for tuber- | % ND) | select 1 more application in future; 4-year | |
| SmithKline Beecham | culosis (amended 3/97 to | collaboration; SmithKline licensed rights | ||
| plc; NYSE:SBH; U.K.) | include antigens for use in | to Corixa's HER-2/neu vaccine for breast | ||
| vaccines for breast and | and ovarian cancer and its breast cancer | |||
| prostate cancer) to include | antigen mammaglobin; except for tuber- | |||
| vaccines for ovarian and | culosis vaccine, SmithKline gets exclusive | |||
| colon carcinoma as well as | worldwide rights to all vaccine products; | |||
| for infectious diseases | SmithKline also has option on nonexclusive | |||
| Chlamydia trachomatis | license to Corixa's LeiF adjuvant and its | |||
| and C. pneumoniae | microsphere delivery technology; Corixa | |||
| gets $49M committed funding over 4 years | ||||
| (which includes a $2.5M equity purchase | ||||
| now and $2.5M in the future, both at premi- | ||||
| um); Corixa gets milestones of $150M, as | ||||
| well as royalties; Corixa retains right to | ||||
| form non-vaccine partnerships for these | ||||
| antigens; transaction subject to antitrust | ||||
| considerations (10/98) | ||||
| Corvas | Ortho Clinical | Restructured agreement | $1M | Original 1992 agreement concerned |
| International Inc. | Diagnostics Inc. | that supercedes 1992 | supply of thromboplastin formulations | |
| (unit of Johnson & | agreement for license to | to Ortho; Corvas has now licensed the | ||
| Johnson; NYSE:JNJ) | Corvas' recombinant | diagnostic applications of its thrombo- | ||
| thromboplastin for use | plastin; Ortho also gets certain licenses | |||
| in diagnostics | related to production of recombinant | |||
| tissue factor; Corvas gets $1M for | ||||
| these licenses and will continue to get | ||||
| royalties (12/98) | ||||
| Schering-Plough | Extension of 6/97 | $3M | Schering-Plough will support preclinical | |
| Corp. (NYSE:SGP) | collaboration on oral | development through 9/99 and provide | ||
| anticoagulants based on | additional $3M in funding (12/98) | |||
| protease inhibitors | ||||
| Gene Logic Inc. | The Procter & | Expansion of 6/97 | ND | Expansion will result in doubling of |
| Gamble Co. | collaboration on thera- | Gene Logic's annual revenues from | ||
| (NYSE:PG) | peutic targets for heart | collaboration; Procter & Gamble gets | ||
| failure (via Gene Logic's | access to databases and will pay annual | |||
| READS gene expression | fees; Gene Logic also gets milestones | |||
| technology for database of | and royalties; the partners can now | |||
| differential gene expres- | work together on any disease indication; | |||
| sion) to include target in | Gene Logic can work with 3rd parties | |||
| osteoporosis | on specific indications (12/98) | |||
| Rhone-Poulenc | Expansion of 9/97 | ND | The original agreement was between | |
| Rorer Inc. | alliance to conduct p53 | Rhone-Poulenc Rorer and OncorMed | ||
| (subsidiary of | testing for clinical trials | (which Gene Logic acquired in 9/98); | ||
| Rhone-Poulenc SA; | of adenoviral p53 gene | this is expansion of alliance to analyze | ||
| NYSE:RP; France) | therapy for cancer | genes for gene therapy clinical trials; | ||
| financial details ND (11/98) | ||||
| GeneMedicine Inc. | Merck & Co. Inc. | Expansion of 12/97 | ND | Collaboration initially focused on 2 |
| (NYSE:MRK) | collaboration to evaluate | therapeutic applications; it has now been | ||
| GeneMedicine's Gene- | expanded to include 3 applications; | |||
| Switch technology (to | further details ND (11/98) | |||
| control gene expression) | ||||
| with Merck's vector system | ||||
| for gene-based therapies | ||||
| Genome | Schering-Plough | Acceleration of 12/96 | ND | Asthma genetics program is ahead of |
| Therapeutics | Corp. (NYSE:SGP) | collaboration to identify | schedule; companies have enlarged | |
| Corp. | genes involved in suscep- | program substantially and have moved | ||
| tibility to asthma | up the time lines (11/98) | |||
| Incyte Pharma- | Pfizer Inc. | Expansion of 6/94 genom- | ND | Companies already extended and |
| ceuticals Inc. | (NYSE:PFE) | ic database partnership to | expanded agreement in 2/98; now, | |
| include Incyte's LifeTools | Pfizer will use Incyte's LifeTools and | |||
| bioinformatics software | LifeArray to support its global research | |||
| and LifeArray microarray | programs; details ND (9/98) | |||
| data analysis and manage- | ||||
| ment software | ||||
| Inhale Therapeutic | Baxter International | Amendment of terms of | ND | Companies intend to find 3rd party to |
| Systems Inc. | Inc. (NYSE:BAX) | 3/96 collaboration to use | further develop and commercialize | |
| Inhale's dry-powder pul- | an undisclosed compound; Baxter will | |||
| monary delivery system | continue to provide funding in prepara- | |||
| for non-peptide, non- | tion for Phase II trials while 3rd party | |||
| protein drug candidates | is identified; product falls outside Bax- | |||
| ter's current business focus; other 2 | ||||
| compounds in collaboration will remain | ||||
| and may be developed in future (10/98) | ||||
| Medarex Inc. | Merck KGaA | Option to expand 4/94 | $1.5M | Merck paid $1.5M to obtain exclusive |
| (Germany) | collaboration on Meda- | option on worldwide licensing rights to | ||
| rex's MDX-477 bispecific | product; Medarex would retain U.S. | |||
| antibody for certain cancers | rights; Merck will fully fund Phase II | |||
| (targets epidermal growth | trials (12/98) | |||
| factor receptor; currently | ||||
| in Phase II trials for head | ||||
| and neck cancer) | ||||
| Microcide | Ortho-McNeil | Extension of 10/95 collab- | ND | Companies will continue joint develop- |
| Pharmaceuticals | Pharmaceuticals and | oration on therapeutics for | ment of beta-lactam compounds; John- | |
| Inc. | the R.W. Johnson | Gram-positive bacterial | son & Johnson will support research | |
| Pharmaceutical | infections, especially drug- | for additional 8-14 months; the duration | ||
| Research Institute | resistant strains; focus on | and amount of funding will depend on | ||
| (units of Johnson & | beta-lactam compounds | selection of 1 additional compound for | ||
| Johnson; NYSE:JNJ) | development by 12/31/98; Microcide | |||
| regained rights to its antibiotic potentia- | ||||
| tor technologies and compounds (10/98) | ||||
| Myriad Genetics | Bayer Corp. | Extension of 9/95 alliance | $12.2M | Bayer extended collaboration until 9/02; |
| Inc. | (unit of Bayer AG; | to discover genes that | Myriad has made significant progress | |
| Germany) | predispose individuals to | toward isolating disease-causing genes; | ||
| obesity, osteoporosis and | Myriad will get additional $6.2M in | |||
| asthma | committed research funds plus $6M in | |||
| milestones over next 2 years (12/98) | ||||
| Neurogen Corp. | Pfizer Inc. | Extension and expansion | $12.5M | Collaboration extended for 2 years; |
| (NYSE:PFE) | of collaborations on small- | Neurogen gets $6.25M per year in | ||
| molecule drugs that act on | additional research funds (11/98) | |||
| specific GABA receptors | ||||
| in brain; on drugs for | ||||
| anxiety and cognition | ||||
| (from 2/92) and drugs for | ||||
| sleep disorders (from 6/94); | ||||
| added depression as new | ||||
| target | ||||
| Xenova Group | Parke-Davis | Extension of 5/97 drug | ND | Xenova provided natural product extracts |
| plc (U.K.) | (division of | discovery collaboration | for screening, which Parke-Davis has done, | |
| Warner-Lambert | based on Xenova's | identifying potential hits from which | ||
| Co.; NYSE:WLA) | NatChem natural products | Xenova will now isolate and identify | ||
| library | active chemicals; Xenova gets certain | |||
| additional payments (10/98) | ||||
| II. TERMINATED AGREEMENTS | ||||
| Alkermes Inc. | The R.W. Johnson | Termination of 12/96 | Companies reached mutual decision to | |
| Pharmaceutical | collaboration on use of | terminate collaboration; Alkermes | ||
| Research Institute | Alkermes' ProLease drug | regains all rights licensed to Pharma- | ||
| (unit of Johnson & | delivery system to develop | ceutical Research Institute, which has | ||
| Johnson; NYSE:JNJ) | sustained-release formula- | discontinued product development | ||
| tion of undisclosed drug | (11/98) | |||
| for treating hormone- | ||||
| mediated disorders | ||||
| Schering-Plough | Termination of 1/92 | Companies reached mutual decision | ||
| Corp. (NYSE:SGP) | agreement on use of | to terminate collaboration; Alkermes | ||
| Alkermes' ProLease drug | regains all rights licensed to Schering- | |||
| delivery system to develop | Plough; further details ND (11/98) | |||
| sustained-release formula- | ||||
| tion of Intron A (recombi- | ||||
| nant interferon alfa-2b) | ||||
| Allelix Biopharma- | Astra AB | Termination of 6/96 | As a result of corporate restructuring | |
| ceuticals Inc. | (Sweden) | agreement to develop | at Astra, this program no longer fits; | |
| (Canada) | ALX1-11 (recombinant | Allelix reacquired all product rights, | ||
| human parathyroid | including assets, know-how and pro- | |||
| hormone) for treating | prietary rights; Allelix will assume | |||
| osteoporosis (currently | responsibility for product development | |||
| in Phase II trials) | (9/98) | |||
| Ergo Science | The R.W. Johnson | Termination of 2/98 | FDA denied approval of Ergoset in | |
| Corp. | Pharmaceutical | collaboration on | 11/98, after which Johnson & Johnson | |
| Research Institute | Ergoset Tablets (bromo- | terminated collaboration (12/98) | ||
| and Ortho-McNeil | criptine mesylate; dopa- | |||
| Pharmaceutical Inc. | mine agonist) and other | |||
| (units of Johnson | products for treating | |||
| & Johnson; NYSE:JNJ) | Type II diabetes and | |||
| obesity | ||||
| Inex Pharma- | Schwarz Pharma | Termination of 3/98 | Drug failed to show benefit in Phase II | |
| ceuticals Corp. | AG (Germany) | collaboration to develop | trial; companies discontinued develop- | |
| (TSE:IEX; Canada) | antisense drug INX-3280 | ment in Europe and North America; | ||
| (blocks function of c-myc | Inex will not continue product develop- | |||
| gene) for treating cardio- | ment on its own (10/98) | |||
| vascular restenosis | ||||
| Intercardia Inc. | Astra Pharma- | Termination of 12/95 | As a result of corporate restructuring at | |
| ceuticals LP | agreement on Bextra | Astra (it bought out Merck's share of Astra | ||
| (formerly Astra | (bucindolol HCl) for | Merck), Astra's product line now includes | ||
| Merck Inc.) | treating congestive heart | a competing product (Toprol-XL); agreement | ||
| failure (currently in | terminated by mutual agreement, due to | |||
| Phase III trials) | non-compete clause in terms of original | |||
| deal; Intercardia regains all rights, material | ||||
| and information relating to product, | ||||
| plus termination fee (9/98) | ||||
| NeoRx Corp. | Janssen | Termination of 8/97 | Janssen will terminate agreement at | |
| Pharmaceutica NV | collaboration on NeoRx's | year-end 1998, but is currently com- | ||
| (Belgium; unit of | radioimmunotherapy prod- | pleting Phase II trials in advanced | ||
| Johnson & Johnson; | uct Avicidin (for treating | colon and prostate cancer; patients | ||
| NYSE:JNJ) | solid tumors) | exhibited high incidence of unaccept- | ||
| able diarrhea; all rights to product and | ||||
| underlying pretargeting technology | ||||
| revert to NeoRx, along with all data | ||||
| generated by study (9/98) | ||||
| Schwarz Pharma | Termination of 4/97 | Schwarz ceased product development, | ||
| AG (Germany) | collaboration on NeoRx's | citing need for more studies with a new | ||
| Biostent (combination | catheter and delays in the project; | |||
| drug/device) for treating | NeoRx has no plans to conduct Phase II | |||
| restenosis following | trials without a partner (11/98) | |||
| balloon angioplasty | ||||
| (Phase I trials completed) | ||||
| Sonus Pharma- | Daiichi | Termination of 3/95 | Daiichi took product through Phase I | |
| ceuticals Inc. | Pharmaceutical | license agreement on | trials in Japan, completed in 12/97, but | |
| Co. Ltd. (Japan) | EchoGen ultrasound | no further clinical development since | ||
| contrast agent for intra- | that time; Sonus terminated agreement | |||
| venous myocardial con- | and is seeking another development | |||
| trast echocardiography | partner (11/98) | |||
| NOTES: | ||||
| # This chart contains information on modified and terminatedagreements only, covering the time period between 9/23/98 and 12/24/98.It does not include arrangements that are classed strictly as production,marketing and/or distribution agreements, nor does it include any collaborationsthat involve agricultural product development. | ||||
| For a chart listing new collaborations between biotechcompanies and big pharma for the same time period (9/23/98 12/24/98),see the 1/4/99 issue of BioWorld Financial Watch. | ||||
| ND = Not disclosed, reported and/or available; TSE = TorontoStock Exchange | ||||
| * Private companies are indicated with an asterisk. | ||||
| ** Unless otherwise notes, the trading symbols for publicbiotechnology companies can be found by referring to the BioWorld Stockreport For Public Biotechnology Companies on pp. 12-13. | ||||
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