| 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 joint | ND | This joint venture was expanded |
| Sciences Inc. | plc (U.K.) | venture to commercial- | once in 1/98 to include Derma- | |
| ize Dermagraft (for | graft-TC for all wound care appli- | |||
| diabetic foot ulcers and | cations outside the U.S. and all | |||
| venous and pressure | non-burn wound care applications | |||
| ulcers) and Dermagraft- | in U.S.; now, Smith & Nephew | |||
| TC (for full and partial- | will market Dermagraft-TC (to be | |||
| thickness burns) to | renamed TransCyte) for burns in | |||
| include new territory | the U.S. (8/98) | |||
| Affymetrix Inc. | American Home | Exercise of option to | ND | American Home exercised option |
| Products Corp. | subscribe to Affymetrix's | under 1/98 agreement between its | ||
| (NYSE:AHP) | Easy Access program | subsidiary Genetics Institute and | ||
| for GeneChip expression | Affymetrix; American Home and | |||
| probe arrays | its affiliates get broad access to | |||
| custom and standard GeneChips | ||||
| plus instrumentation and software; | ||||
| Affymetrix gets subscription fees | ||||
| and fixed per-chip fees (9/98) | ||||
| ArQule Inc. | Amersham Pharma- | Extension of joint | ND | This is the 4th extension; further |
| cia Biotech | collaboration to develop | details ND (8/98) | ||
| advanced separations | ||||
| products, especially | ||||
| affinity ligands via | ||||
| ArQule's combinatorial | ||||
| chemistry; agreement | ||||
| dates from 3/95 | ||||
| Aurora | Parke-Davis | Expansion of 9/97 | $9M | Wyeth-Ayerst will pay $9M over |
| Biosciences Corp. | (division of Warner- | agreement on Aurora's | 15 months for the new system | |
| Lambert Co.; NYSE: | ultra-high-throughput | (8/98) | ||
| WLA) | screening system | |||
| (UHTSS) to include | ||||
| development of auto- | ||||
| mated master com- | ||||
| pound storage system | ||||
| for long-term housing | ||||
| of chemical and bio- | ||||
| logical compounds | ||||
| Cell Therapeutics | Ortho Biotech Inc./ | Restructuring of 11/96 | ND | Due to negative results of 1st |
| Inc. | The R.W. Johnson | R&D and marketing | Phase III trial, the regulatory time- | |
| Pharmaceutical | agreement on lisofylline | line for this drug has been altered; | ||
| Research Institute | (anti-inflammatory drug | Cell Therapeutics will now con- | ||
| (both are affiliates | for reducing toxicities | trol and fund product development; | ||
| of Johnson & John- | from radiation and | Johnson & Johnson will pay its | ||
| son; NYSE:JNJ) | chemotherapy in cancer | share through 12/31/98; if new | ||
| patients) | Phase III trial is positive, Johnson | |||
| & Johnson has option of resuming | ||||
| responsibility for product develop- | ||||
| ment and marketing; if it exercises | ||||
| option, Cell Therapeutics gets | ||||
| additional payments; if not, then | ||||
| Cell Therapeutics can license prod- | ||||
| uct to other 3rd parties (7/98) | ||||
| Cima Labs Inc. | Novartis Consumer | Novartis exercised | ND | ND (7/98) |
| Health Inc. (division | option under 12/97 | |||
| of Novartis AG; | agreement to license | |||
| Switzerland) | consumer products | |||
| developed via OraSolv | ||||
| fast-dissolve technology | ||||
| Corixa Corp. | Pasteur Merieux | Extension of 3/97 | ND | This collaboration was already |
| Connaught (unit | research agreement and | extended with new options in 1/98, | ||
| of Rhone-Poulenc | license option on use | but those options were to expire; | ||
| Group; France) | of Corixa's protein | Pasteur Merieux extended its | ||
| adjuvant LeIF (Leish- | options until 12/31/98 to license | |||
| mania elongation | LeIF exclusively for use in influ- | |||
| initiation factor) in | enza and respiratory syncytial | |||
| vaccines for infectious | virus vaccines and nonexclusively | |||
| diseases | for use in HIV, tuberculosis and | |||
| malaria vaccines (8/98) | ||||
| SmithKline Beech- | Extension of 10/95 | ND | SmithKline will provide additional | |
| am Biologicals SA | collaboration on T-cell | research funding through 5/99 and | ||
| (Belgium; subsid- | active recombinant | gets exclusive option to license | ||
| iary of SmithKline | subunit vaccines for | Corixa's tuberculosis antigens for | ||
| Beecham plc; | infectious diseases, | use as vaccine through 8/99; if it | ||
| NYSE:SBH; U.K.) | specifically tuberculosis | exercises option, Corixa gets fee | ||
| plus milestones; SmithKline gets | ||||
| exclusive worldwide rights except in | ||||
| Japan, where Corixa gets co-exclu- | ||||
| sive rights (8/98) | ||||
| Desmos Inc.* | Baxter Healthcare | Renewal and extension | ND | ND (7/98) |
| Corp. (subsidiary of | of 9/97 collaboration on | |||
| Baxter International | use of Desmos' extra- | |||
| Inc.; NYSE:BAX) | cellular matrix as bio- | |||
| coating for percutaneous | ||||
| implants used in renal | ||||
| therapy | ||||
| GeneMedicine Inc. | Corange Interna- | Expansion of 7/95 | ND | Research term of collaboration |
| tional Ltd. (unit of | collaboration on non- | extended until 2/02; companies will | ||
| Roche Holdings | viral gene therapies for | work exclusively together on gene | ||
| Ltd.; Switzerland) | certain cancers to cover | therapies using the 3 genes; focus | ||
| all human cancer indica- | on Phase II trial of IL-2 in head and | |||
| tions for gene medicines | neck cancer and preclinical through | |||
| using genes for interleu- | Phase I/II trials of other 2 genes (same | |||
| kin-2 (IL-2), interferon- | indication); on successful completion | |||
| alpha (IFN-a) and inter- | of 1 clinical trial, GeneMedicine has | |||
| leukin-12 (IL-12); genes | option to share development costs | |||
| used alone or in com- | in exchange for 50% of profits or to get | |||
| bination | royalties on worldwide sales; Roche | |||
| will convert additional equity pay- | ||||
| ments under 7/95 agreement into | ||||
| research and milestone payments; | ||||
| GeneMedicine can partner with other | ||||
| firms in gene therapy for cancer using | ||||
| different genes (8/98) | ||||
| Genzyme | Eli Lilly and Co. | Expansion of 3/98 | $22M | Lilly's option to license protein |
| Transgenics Corp. | (NYSE:LLY) | feasibility agreement to | expires 12/99; until then, Genzyme | |
| produce a transgenic | Transgenics will get $1M develop- | |||
| therapeutic protein | ment funding; on execution of | |||
| option, Genzyme Transgenics gets | ||||
| funding and milestones of $22M; | ||||
| Lilly gets worldwide rights; Gen- | ||||
| zyme Transgenics will manufacture | ||||
| protein and gets royalties (7/98) | ||||
| Hybridon Inc. | G.D. Searle & Co. | Extension and expan- | ND | Searle will continue to support |
| (OTC Bulletin | (subsidiary of Mon- | sion of 1/96 collabor- | research through 1/00; Searle has | |
| Board:HYBN) | santo Co.; NYSE: | ation on antisense drugs | option of designating additional | |
| MTC) | for inflammatory disease | molecular targets; companies also | ||
| to include more targets | initiated program focused on onco- | |||
| in cardiovascular disease | gene MDM2 (inhibits apoptosis) | |||
| and cancer, including | (7/98) | |||
| MDM2 oncogene | ||||
| Immunex Corp. | American Home | Restructuring of prod- | ND | Immunex no longer obligated to fund |
| Products Corp. | uct rights agreements | certain oncology R&D at American | ||
| (NYSE:AHP) | and termination of | Home's subsidiary American Cyanamid; | ||
| oncology agreement; | Immunex gets worldwide rights to | |||
| especially concerns | Leukine and 3 drugs still in clinic | |||
| Leukine, Mobist (FLT-3 | (to which American Home had held | |||
| ligand), IL-15 and | rights outside North America); Immu- | |||
| CD40 ligand | nex will pay royalties to American | |||
| Home on ex-North American sales; | ||||
| American Home has option to acquire | ||||
| rights to 4 future Immunex products; | ||||
| Immunex can convert 2 of those calls | ||||
| and then pay American Home mile- | ||||
| stones and royalties; for exercised | ||||
| call, Immunex gets fees, milestones | ||||
| and royalties (7/98) | ||||
| Incyte | Novartis AG | Expansion of 6/97 | ND | This is the 2nd expansion of the |
| Pharmaceuticals | (Switzerland) | database partnership to | partnership; Novartis gets data | |
| Inc. | include Incyte's gene | from DNA microarrays from the | ||
| expression microarray | UniGEM product line as well as | |||
| technology | data from custom microarrays; | |||
| Incyte gets access fees and per- | ||||
| experiment fees (7/98) | ||||
| Pharmacopeia Inc. | Berlex Laboratories | Expansion of 2/95 | ND | Pharmacopeia will get additional |
| Inc. (subsidiary of | agreement on use of | research funding, milestones and | ||
| Schering AG; | combinatorial chemistry | royalties (8/98) | ||
| Germany) | and high-throughput | |||
| screening for drug leads | ||||
| for multiple sclerosis | ||||
| to pursue chemical | ||||
| optimization of lead | ||||
| compound against | ||||
| additional target | ||||
| Organon NV | Expansion of 5/96 | ND | Pharmacopeia will get additional | |
| (the Netherlands) | agreement on use of | research funding, milestones and | ||
| combinatorial chemistry | royalties (8/98) | |||
| and high-throughput | ||||
| screening for drug leads | ||||
| to include development | ||||
| of compound against | ||||
| additional target | ||||
| Phytera Inc.* | Tsumura & Co. | Extension and expansion | ND | Collaboration extended through |
| (Japan) | of 6/96 collaboration | 6/00; Phytera gets research funds | ||
| on use of Phyton's plant | and milestones; companies co-own | |||
| cell culture extract librar- | products; Phytera gets exclusive | |||
| ies to screen for small mole- | rights in North America; Tsumura | |||
| cules to treat rheumatoid | gets exclusive rights elsewhere; | |||
| arthritis and allergies; will | companies will pay each other | |||
| now also screen Phytera's | royalties (8/98) | |||
| marine microorganism | ||||
| extract libraries | ||||
| Regeneron | Sumitomo Pharma- | Expansion of 6/94 col- | $5M | Sumitomo licensed the product |
| Pharmaceuticals | ceuticals Co. Ltd. | laboration on BDNF | for developing in Japan; Regeneron | |
| Inc. | (Japan) | (brain-derived neuro- | gets initial $5M payment plus | |
| trophic factor) for | milestones and royalties (8/98) | |||
| treating amyotrophic | ||||
| lateral sclerosis | ||||
| II. TERMINATED AGREEMENTS | ||||
| Cambridge | Boehringer Ingel- | Termination of 1/95 | — | Based on further evaluation of |
| NeuroScience Inc. | heim International | collaboration on Cere- | negative Phase III interim results, | |
| GmbH (Germany) | stat (NMDA ion- | companies have terminated collab- | ||
| channel blocker) for | oration but are still negotiating | |||
| traumatic brain | specific terms and conditions (7/98) | |||
| injury and stroke | ||||
| CoCensys Inc. | G.D. Searle & Co. | Termination of 5/96 | — | Searle ended agreement but pro- |
| (subsidiary of Mon- | collaboration on | vided no explanation; CoCensys | ||
| santo Co.; NYSE: | CCD 3693 (synthetic | retains all rights to compounds in | ||
| MTC) | epalon or neuroactive | this program (7/98) | ||
| steroid) for treating | ||||
| insomnia (Phase I | ||||
| trials completed) | ||||
| Corvas | Schering-Plough | Termination of 12/94 | — | Companies terminated this pro- |
| International Inc. | Corp. (NYSE:SGP) | collaboration on orally | gram after disappointing results of | |
| bioavailable thrombin | a Phase I trial; the 2 other research | |||
| inhibitors for prevent- | programs (on inhibitors of Factor | |||
| ing and treating cardio- | Xa and hepatitis C virus) remain | |||
| vascular disorders | intact (8/98) | |||
| Diatide Inc. | Nycomed Amer- | Termination of 8/95 | — | Nycomed will discontinue R&D |
| sham plc (U.K.) | option and develop- | payments for early-stage products | ||
| ment agreement on | as of 1/31/99; Diatide regains U.S. | |||
| early-stage imaging | rights to all non-optioned products; | |||
| products | decision does not affect license | |||
| and co-promotion agreements on | ||||
| AcuTect and P829 imaging prod- | ||||
| ucts (8/98) | ||||
| Gilead Sciences | Glaxo Wellcome | Termination of 7/90 | — | The companies jointly decided to |
| Inc. | plc (NYSE:GLX; | collaboration on genetic | end this collaboration (under a | |
| U.K.) | code blockers (including | 3/96 extension, Glaxo had option | ||
| antisense and triple- | to terminate after 2 years); each | |||
| helix compounds) | company retains rights to jointly | |||
| developed technology as well as | ||||
| its own research results (6/98) | ||||
| MorphoSys | Pharmacia & | Termination of 3/97 | — | Pharmacia & Upjohn made stra- |
| GmbH* | Upjohn Inc. | research collaboration | tegic decision to focus its research | |
| (Germany) | (NYSE:PNU; | on use of MorphoSys' | in areas other than inflammation; | |
| U.K.) | human antibody library | plans to continue into 2nd phase of | ||
| and phage-based screen- | collaboration were suspended | |||
| ing technology to iden- | (8/98) | |||
| tify lead compounds and | ||||
| therapeutic targets for | ||||
| inflammation and other | ||||
| diseases | ||||
| Ophidian | Eli Lilly and Co. | Termination of 5/96 | — | Lilly said it will discontinue pro- |
| Pharmaceuticals | (NYSE:LLY) | collaboration on avian | gram; Ophidian regains all rights | |
| Inc. | polyclonal antibody to | to product (9/98) | ||
| neutralize toxins | ||||
| secreted by Clostridium | ||||
| difficile (gastrointes- | ||||
| tinal infection; Phase I | ||||
| trial completed) | ||||
| Neurogen Corp. | Schering-Plough | Conclusion of joint | — | Schering-Plough moved the re- |
| Corp. (NYSE:SGP) | research phase of 6/95 | search in-house; if drug candidates | ||
| collaboration on small-mol- | progress through clinic, Neurogen | |||
| ecule drugs that modulate | gets milestones and royalties; | |||
| dopamine receptor sub- | Neurogen retains option to manu- | |||
| types for treating | facture products for U.S. market | |||
| schizophrenia | (7/98) | |||
| NOTES: | ||||
| # This chart contains information on modified and terminated agreements only, covering the time period between 6/16/98 and 9/21/98. 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 (6/16/98 - 9/21/98), see the 9/28/98 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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