Page 71 - Ethical Guidelines for Conducting Research Studies Involving Human Subjects
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7.      Physicians should disclose all clinically relevant findings to
                                         the woman or couple, including the full range of variability
                                         in  the  manifestations  of  the  condition  under  discussion
                                         (autonomy).
                                 8.      The woman's and/or couple's choices in a pregnancy with an
                                         affected fetus should be respected and protected, within the
                                         framework of the family and of the laws, culture and social
                                         structure  of  the  country.  The  couple,  not  the  health
                                         professional,  should  make  the  choice  (autonomy).  (WHO,
                                         2003, ICMR, 2006, India)

                                 The  following  points  should  be  noted  and  reflected  in
                                 guidelines:

                                 a.      Prenatal sex determination will not be allowed.

                                 b.      Termination of pregnancy for a genetic cause has to      be
                                         restricted by strict medical supervision.
                                 c.      BMRC  should  be  aware  for  any  uncertain  future
                                         developments and research applications in these  fields.

                                 d.      Genetic manipulation to modify the genes of a fetus      or
                                         pre-embryo will not be allowed.

                          13.8  GENE THERAPY


                          The term “gene therapy”, when it is used subsequently, will mean somatic
                          cell gene therapy only. BMRC would not be expected to receive, and should
                          not approve, research proposals for the introduction of DNA and RNA into
                          germ  (reproductive)  cells  or  embryos.  “Gene  therapy”  will  also  refer  to
                          research  protocols  with  either  therapeutic  or  non-therapeutic  aims.
                          Therapeutic  research  is  conducted  with  the  intent  of  providing  a  direct
                          benefit  to  research  participants,  while  non-therapeutic  research  is
                          conducted  with  the  intent  to  derive  knowledge  and  not  to  be  of  direct
                          benefit to research participants (More on Gene therapy ANNEXURE-B).

                          A research proposal must be evaluated based on medical, scientific, ethical
                          and  safety  aspects.  The  proposal  must  be  first  approved  by  the  concern
                          institutional  biosafety  committee  before  submitting  to  NREC  of  BMRC.
                          The following also need to be taken into account when protocols for gene
                          therapy are being considered by BMRC:

                          a.     The balance of potential risks and benefits associated with the gene
                                 therapy  experiment.  Diseases  for  which  gene  therapy  is  being
                                 considered  should  be  those  which  impose  a  severe  burden  on
                                 affected  individuals  and  for  which  there  is  no  treatment  or  only
                                 inadequate  treatment.  There  is  accumulating  evidence  that  gene
                                 therapy is relatively safe for humans, but the choice of diseases for



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